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	<title>Recall Newsletter</title>
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	<link>http://www.recallnewsletter.com</link>
	<description>All of Your Recall News And Alerts In One Easy To Use Place Or Sent To You By Email</description>
	<lastBuildDate>Fri, 03 Sep 2010 18:48:04 +0000</lastBuildDate>
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		<title>Cibo Vita issues Allergy Alert on Undeclared Sulfites in Mediterranean Mix of Woodpecker Brand</title>
		<link>http://www.recallnewsletter.com/cibo-vita-issues-allergy-alert-on-undeclared-sulfites-in-mediterranean-mix-of-woodpecker-brand</link>
		<comments>http://www.recallnewsletter.com/cibo-vita-issues-allergy-alert-on-undeclared-sulfites-in-mediterranean-mix-of-woodpecker-brand#comments</comments>
		<pubDate>Fri, 03 Sep 2010 18:48:04 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/cibo-vita-issues-allergy-alert-on-undeclared-sulfites-in-mediterranean-mix-of-woodpecker-brand</guid>
		<description><![CDATA[Cibo Vita, 280 N. Midland Ave Saddle Brook, NJ 07663 is recalling Mediterranean Mix of Woodpecker brand because it may contain undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product. The recalled Mediterranean Mix, in plastic containers of 8.5 OZ was [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Cibo Vita, 280 N. Midland Ave Saddle Brook, NJ 07663 is recalling Mediterranean Mix of Woodpecker brand because it may contain undeclared sulfites. People who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.</p>
<p>The recalled Mediterranean Mix, in plastic containers of 8.5 OZ was sold to the list of the attached customers.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224929.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Good Taste Noodle MFG Recalls &quot;Egg Noodles and Wonton Skins&quot; Because Of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/good-taste-noodle-mfg-recalls-egg-noodles-and-wonton-skins-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/good-taste-noodle-mfg-recalls-egg-noodles-and-wonton-skins-because-of-possible-health-risk#comments</comments>
		<pubDate>Fri, 03 Sep 2010 12:24:03 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/good-taste-noodle-mfg-recalls-egg-noodles-and-wonton-skins-because-of-possible-health-risk</guid>
		<description><![CDATA[Good Taste Noodle MFG. of Chicago, IL, is recalling its “EGG NOODLES and WONTON SKINS, labeled with production date from June 19, 2010 to August 19, 2010”, because they have the potential to be contaminated with salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Good Taste Noodle MFG. of Chicago, IL, is recalling its “EGG NOODLES and WONTON SKINS, labeled with production date from June 19, 2010 to August 19, 2010”, because they have the potential to be contaminated with salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune system. Healthy persons infected with salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224843.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>ADVENTURE ( 10V391000 )</title>
		<link>http://www.recallnewsletter.com/adventure-10v391000</link>
		<comments>http://www.recallnewsletter.com/adventure-10v391000#comments</comments>
		<pubDate>Fri, 03 Sep 2010 10:00:14 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/adventure-10v391000</guid>
		<description><![CDATA[Dated: SEP 01, 2010 ADVENTURER IS RECALLING CERTAIN MODEL YEAR 2011 ADVENTURER MOTOR HOMES AND TRUCK CAMPERS EQUIPPED WITH SUBURBAN GAS COOK STOVES WITH SEALED BURNERS. THE UNITS INVOLVED USE AN ALUMINUM TUBE TO CARRY L&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: SEP 01, 2010 ADVENTURER IS RECALLING CERTAIN MODEL YEAR 2011 ADVENTURER MOTOR HOMES AND TRUCK CAMPERS EQUIPPED WITH SUBURBAN GAS COOK STOVES WITH SEALED BURNERS.  THE UNITS INVOLVED USE AN ALUMINUM TUBE TO CARRY L&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V391000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>ITASCA ( 10V390000 )</title>
		<link>http://www.recallnewsletter.com/itasca-10v390000</link>
		<comments>http://www.recallnewsletter.com/itasca-10v390000#comments</comments>
		<pubDate>Fri, 03 Sep 2010 10:00:14 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/itasca-10v390000</guid>
		<description><![CDATA[Dated: SEP 01, 2010 WINNEBAGO IS RECALLING CERTAIN MODEL YEAR 2011 VISTA AND ITASCA SUNSTAR MOTOR HOMES MANUFACTURED FROM MARCH 16, 2010 THROUGH AUGUST 12, 2010. THESE VEHICLES MAY HAVE THE POTENTIAL FOR A CABLE THAT PO&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: SEP 01, 2010 WINNEBAGO IS RECALLING CERTAIN MODEL YEAR 2011 VISTA AND ITASCA SUNSTAR MOTOR HOMES MANUFACTURED FROM MARCH 16, 2010 THROUGH AUGUST 12, 2010.  THESE VEHICLES MAY HAVE THE POTENTIAL FOR A CABLE THAT PO&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V390000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>WINNEBAGO ( 10V390000 )</title>
		<link>http://www.recallnewsletter.com/winnebago-10v390000</link>
		<comments>http://www.recallnewsletter.com/winnebago-10v390000#comments</comments>
		<pubDate>Fri, 03 Sep 2010 10:00:14 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/winnebago-10v390000</guid>
		<description><![CDATA[Dated: SEP 01, 2010 WINNEBAGO IS RECALLING CERTAIN MODEL YEAR 2011 VISTA AND ITASCA SUNSTAR MOTOR HOMES MANUFACTURED FROM MARCH 16, 2010 THROUGH AUGUST 12, 2010. THESE VEHICLES MAY HAVE THE POTENTIAL FOR A CABLE THAT PO&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: SEP 01, 2010 WINNEBAGO IS RECALLING CERTAIN MODEL YEAR 2011 VISTA AND ITASCA SUNSTAR MOTOR HOMES MANUFACTURED FROM MARCH 16, 2010 THROUGH AUGUST 12, 2010.  THESE VEHICLES MAY HAVE THE POTENTIAL FOR A CABLE THAT PO&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V390000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.recallnewsletter.com/winnebago-10v390000/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>FERRARI ( 10V389000 )</title>
		<link>http://www.recallnewsletter.com/ferrari-10v389000</link>
		<comments>http://www.recallnewsletter.com/ferrari-10v389000#comments</comments>
		<pubDate>Fri, 03 Sep 2010 10:00:13 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/ferrari-10v389000</guid>
		<description><![CDATA[Dated: AUG 31, 2010 FERRARI IS RECALLING CERTAIN MODEL YEAR 2010 458 ITALIA VEHICLES. THE HEAT CREATED BY THE ENGINE COULD CAUSE POSSIBLE DEFORMATION OF THE REAR RIGHT HAND AND LEFT HAND WHEELHOUSE AND HEAT SHIELD ASSEM&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 31, 2010 FERRARI IS RECALLING CERTAIN MODEL YEAR 2010 458 ITALIA VEHICLES.  THE HEAT CREATED BY THE ENGINE COULD CAUSE POSSIBLE DEFORMATION OF THE REAR RIGHT HAND AND LEFT HAND WHEELHOUSE AND HEAT SHIELD ASSEM&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V389000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.recallnewsletter.com/ferrari-10v389000/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Whole Foods Market® Announces Recall of Morningland Dairy and Ozark Hills Farm Cheese</title>
		<link>http://www.recallnewsletter.com/whole-foods-market%c2%ae-announces-recall-of-morningland-dairy-and-ozark-hills-farm-cheese</link>
		<comments>http://www.recallnewsletter.com/whole-foods-market%c2%ae-announces-recall-of-morningland-dairy-and-ozark-hills-farm-cheese#comments</comments>
		<pubDate>Thu, 02 Sep 2010 18:46:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/whole-foods-market%c2%ae-announces-recall-of-morningland-dairy-and-ozark-hills-farm-cheese</guid>
		<description><![CDATA[The following press release was issued by Whole Foods Market&#8217;s North Atlantic Region regarding the voluntary recall of Morningland Dairy of Mountain View, Missouri, Raw Goat Milk Mild Cheddar Cheese. Whole Foods Market’s North Atlantic region is announcing a voluntary recall Morningland Dairy and Ozark Hills Farm Raw Goat Milk Mild Cheddar Cheese due to [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The following press release was issued by Whole Foods Market&#8217;s North Atlantic Region regarding the voluntary recall of Morningland Dairy of Mountain View, Missouri, Raw Goat Milk Mild Cheddar Cheese.</p>
<p>Whole Foods Market’s North Atlantic region is announcing a voluntary recall Morningland Dairy and Ozark Hills Farm Raw Goat Milk Mild Cheddar Cheese due to possible contamination by Listeria and Staphylococcus aureus.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224797.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Toshiba Recalls T Series Notebook Computers Due to Burn Hazard</title>
		<link>http://www.recallnewsletter.com/toshiba-recalls-t-series-notebook-computers-due-to-burn-hazard</link>
		<comments>http://www.recallnewsletter.com/toshiba-recalls-t-series-notebook-computers-due-to-burn-hazard#comments</comments>
		<pubDate>Thu, 02 Sep 2010 15:00:16 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Household Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/toshiba-recalls-t-series-notebook-computers-due-to-burn-hazard</guid>
		<description><![CDATA[The notebook computers can overheat at the notebook&#8217;s plug-in to the AC adapter, posing a burn hazard to consumers. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original recall press release containing complete information, including instructions about what to do [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The notebook computers can overheat at the notebook&#8217;s plug-in to the AC adapter, posing a burn hazard to consumers.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10330.html" target="_blank">View Full Details Of Original CSPC Recall Notice Here</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>KIA ( 10V388000 )</title>
		<link>http://www.recallnewsletter.com/kia-10v388000</link>
		<comments>http://www.recallnewsletter.com/kia-10v388000#comments</comments>
		<pubDate>Thu, 02 Sep 2010 10:00:19 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/kia-10v388000</guid>
		<description><![CDATA[Dated: AUG 31, 2010 HYUNDAI-KIA IS RECALLING CERTAIN MODEL YEAR 2010 SOUL AND MODEL YEAR 2011 SORENTO VEHICLES MANUFACTURED FROM SEPTEMBER 7, 2009 THROUGH JULY 30, 2010. A LIMITED NUMBER OF WIRING HARNESSES SUPPLIED BY &#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 31, 2010 HYUNDAI-KIA IS RECALLING CERTAIN MODEL YEAR 2010 SOUL AND MODEL YEAR 2011 SORENTO VEHICLES MANUFACTURED FROM SEPTEMBER 7, 2009 THROUGH JULY 30, 2010.  A LIMITED NUMBER OF WIRING HARNESSES SUPPLIED BY &#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V388000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.recallnewsletter.com/kia-10v388000/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>KIA MOTOR ( 10V388000 )</title>
		<link>http://www.recallnewsletter.com/kia-motor-10v388000</link>
		<comments>http://www.recallnewsletter.com/kia-motor-10v388000#comments</comments>
		<pubDate>Thu, 02 Sep 2010 10:00:15 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/kia-motor-10v388000</guid>
		<description><![CDATA[Dated: AUG 31, 2010 HYUNDAI-KIA IS RECALLING CERTAIN MODEL YEAR 2010 SOUL AND MODEL YEAR 2011 SORENTO VEHICLES MANUFACTURED FROM SEPTEMBER 7, 2009 THROUGH JULY 30, 2010. A LIMITED NUMBER OF WIRING HARNESSES SUPPLIED BY &#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 31, 2010 HYUNDAI-KIA IS RECALLING CERTAIN MODEL YEAR 2010 SOUL AND MODEL YEAR 2011 SORENTO VEHICLES MANUFACTURED FROM SEPTEMBER 7, 2009 THROUGH JULY 30, 2010.  A LIMITED NUMBER OF WIRING HARNESSES SUPPLIED BY &#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V388000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>HEALTH HAZARD ALERT &#8211; All RAW BEEF PRODUCTS sold on August 6, 2010 from KABUL FARMS, Beverley Hills Drive, North York, Ontario may contain E. coli O157:H7 bacteria</title>
		<link>http://www.recallnewsletter.com/health-hazard-alert-all-raw-beef-products-sold-on-august-6-2010-from-kabul-farms-beverley-hills-drive-north-york-ontario-may-contain-e-coli-o157h7-bacteria</link>
		<comments>http://www.recallnewsletter.com/health-hazard-alert-all-raw-beef-products-sold-on-august-6-2010-from-kabul-farms-beverley-hills-drive-north-york-ontario-may-contain-e-coli-o157h7-bacteria#comments</comments>
		<pubDate>Thu, 02 Sep 2010 06:48:04 +0000</pubDate>
		<dc:creator>CFIA</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Food Recalls Canada CFIA]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/health-hazard-alert-all-raw-beef-products-sold-on-august-6-2010-from-kabul-farms-beverley-hills-drive-north-york-ontario-may-contain-e-coli-o157h7-bacteria</guid>
		<description><![CDATA[The Canadian Food Inspection Agency (CFIA) is warning the public not to consume the raw beef products described&#8230; This is a summary of a recall issued by the Canadian Food Inspection Agency. The link below will take you to the original recall press release containing complete information, including instructions about what to do if you [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The Canadian Food Inspection Agency (CFIA) is warning the public not to consume the raw beef products described&#8230;</p>
<p>This is a summary of a recall issued by the Canadian Food Inspection Agency.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.inspection.gc.ca/english/corpaffr/recarapp/2010/20100901e.shtml" target="_blank">View Full Details Of Original CFIA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>California Firm Recalls Cooked Shredded Pork Skin Products Produced Without Inspection</title>
		<link>http://www.recallnewsletter.com/california-firm-recalls-cooked-shredded-pork-skin-products-produced-without-inspection</link>
		<comments>http://www.recallnewsletter.com/california-firm-recalls-cooked-shredded-pork-skin-products-produced-without-inspection#comments</comments>
		<pubDate>Thu, 02 Sep 2010 03:24:05 +0000</pubDate>
		<dc:creator>USDA FSIS</dc:creator>
				<category><![CDATA[Food Recalls]]></category>
		<category><![CDATA[USDA Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/california-firm-recalls-cooked-shredded-pork-skin-products-produced-without-inspection</guid>
		<description><![CDATA[Trinh Company, a San Jose, Calif., establishment, is recalling approximately 2,070 pounds of cooked shredded pork skin products because the products were produced without the benefit of federal inspection, the U.S. Department of Agriculture&#8217;s Food Safety and Inspection Service (FSIS) announced today. This is a summary of a recall issued by the USDA Food Safety [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Trinh Company, a San Jose, Calif., establishment, is recalling approximately 2,070 pounds of cooked shredded pork skin products because the products were produced without the benefit of federal inspection, the U.S. Department of Agriculture&#8217;s Food Safety and Inspection Service (FSIS) announced today.</p>
<p>This is a summary of a recall issued by the USDA Food Safety and Inspection Service (FSIS).  The link below will take you to the original recall press release, containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fsis.usda.gov/News_&amp;_Events/Recall_051_2010_Release/index.asp" target="_blank">View Full Details Of Original USDA FSIS Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Azteca Linda Corp. Expands Recall of Queso Fresco Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/azteca-linda-corp-expands-recall-of-queso-fresco-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/azteca-linda-corp-expands-recall-of-queso-fresco-because-of-possible-health-risk#comments</comments>
		<pubDate>Wed, 01 Sep 2010 22:48:04 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/azteca-linda-corp-expands-recall-of-queso-fresco-because-of-possible-health-risk</guid>
		<description><![CDATA[Azteca Linda Corp. of Brooklyn, NY, is expanding the 8/24/10 recall of QUESO FRESCO (FRESH WHITE CHEESE (exp. SEP 11 2010) to include expiration date SEP 12 2010. In addition, the firm is recalling Queso El Azteca brand REQUESON (RICOTTA CHEESE) with expiration date SEP 19 2010 because they have the potential to be contaminated with [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Azteca Linda Corp. of Brooklyn, NY, is expanding the 8/24/10 recall of QUESO FRESCO (FRESH WHITE CHEESE (exp. SEP 11 2010) to include expiration date SEP 12 2010. In addition, the firm is recalling Queso El Azteca brand REQUESON (RICOTTA CHEESE) with expiration date SEP 19 2010 because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems&#8230;</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224712.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>P&amp;G Voluntarily Recalls a Small Amount of Dry Cat Food</title>
		<link>http://www.recallnewsletter.com/pg-voluntarily-recalls-a-small-amount-of-dry-cat-food</link>
		<comments>http://www.recallnewsletter.com/pg-voluntarily-recalls-a-small-amount-of-dry-cat-food#comments</comments>
		<pubDate>Wed, 01 Sep 2010 18:48:02 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/pg-voluntarily-recalls-a-small-amount-of-dry-cat-food</guid>
		<description><![CDATA[CINCINNATI, August 31, 2010 &#8211; The Procter &#38; Gamble Company (P&#38;G) is voluntarily recalling a small number of bags from a specific lot of one of its dry cat food products due to potential salmonella exposure. This is a summary of a recall issued by the Food and Drug Administration (FDA). The link below will [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>CINCINNATI, August 31, 2010 &#8211; The Procter &amp; Gamble Company (P&amp;G) is voluntarily recalling a small number of bags from a specific lot of one of its dry cat food products due to potential salmonella exposure.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224675.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Swing Sets Recalled by Kompan Inc. for Repair Due to Fall Hazard</title>
		<link>http://www.recallnewsletter.com/swing-sets-recalled-by-kompan-inc-for-repair-due-to-fall-hazard</link>
		<comments>http://www.recallnewsletter.com/swing-sets-recalled-by-kompan-inc-for-repair-due-to-fall-hazard#comments</comments>
		<pubDate>Wed, 01 Sep 2010 15:48:08 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Children's Toy Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/swing-sets-recalled-by-kompan-inc-for-repair-due-to-fall-hazard</guid>
		<description><![CDATA[The joint connection between the horizontal top beam and the vertical end bracket and support post system can crack and break, posing a fall and impact hazard to users. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original recall press [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The joint connection between the horizontal top beam and the vertical end bracket and support post system can crack and break, posing a fall and impact hazard to users.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10755.html" target="_blank"> View Full Details Of Original CPSC Recall Notice Here</a>, Including Pictures If Any.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>QUESERIA CHIPILO INC. Recalls Cheese Products because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/queseria-chipilo-inc-recalls-cheese-products-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/queseria-chipilo-inc-recalls-cheese-products-because-of-possible-health-risk#comments</comments>
		<pubDate>Wed, 01 Sep 2010 15:00:09 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/queseria-chipilo-inc-recalls-cheese-products-because-of-possible-health-risk</guid>
		<description><![CDATA[August 26, 2010 QUESERIA CHIPILO INC. is announcing a recall of the following cheese products, all date codes up to and including September 26, 2010 – Fresco and Nov 25, 2010 – Oaxaca. This is a summary of a recall issued by the Food and Drug Administration (FDA). The link below will take you to [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>August 26, 2010 QUESERIA CHIPILO INC. is announcing a recall of the following cheese products, all date codes up to and including September 26, 2010 – Fresco and Nov 25, 2010 – Oaxaca.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224627.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Tygacil (tigecycline): Label Change &#8211; Increased Mortality Risk</title>
		<link>http://www.recallnewsletter.com/tygacil-tigecycline-label-change-increased-mortality-risk</link>
		<comments>http://www.recallnewsletter.com/tygacil-tigecycline-label-change-increased-mortality-risk#comments</comments>
		<pubDate>Wed, 01 Sep 2010 14:48:07 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/tygacil-tigecycline-label-change-increased-mortality-risk</guid>
		<description><![CDATA[Healthcare professionals should consider alternatives to Tygacil in patients with severe infections. This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice. View Full Details Of The Original MedWatch Notice Here.]]></description>
			<content:encoded><![CDATA[<p></p><p>Healthcare professionals should consider alternatives to Tygacil in patients with severe infections.</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm224626.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Government of Canada Accepts Recommendations on MS Research</title>
		<link>http://www.recallnewsletter.com/government-of-canada-accepts-recommendations-on-ms-research</link>
		<comments>http://www.recallnewsletter.com/government-of-canada-accepts-recommendations-on-ms-research#comments</comments>
		<pubDate>Wed, 01 Sep 2010 13:48:16 +0000</pubDate>
		<dc:creator>Health Canada</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Health Canada Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/government-of-canada-accepts-recommendations-on-ms-research</guid>
		<description><![CDATA[The Honourable Leona Aglukkaq, Minister of Health, today accepted the recommendations on Multiple Sclerosis (MS) research recently presented to her by Canadian Institutes of Health Research (CIHR) President Dr. Alain Beaudet. These recommendations are based on a thorough review of the current state of science conducted at an August 26, 2010, meeting of leading North [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The Honourable Leona Aglukkaq, Minister of Health, today accepted the recommendations on Multiple Sclerosis (MS) research recently presented to her by Canadian Institutes of Health Research (CIHR) President Dr. Alain Beaudet. These recommendations are based on a thorough review of the current state of science conducted at an August 26, 2010, meeting of leading North American MS experts.</p>
<p>This is a summary of a recall issued by Health Canada.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.hc-sc.gc.ca/ahc-asc/media/nr-cp/_2010/2010_148-eng.php" target="_blank"><br />
View Full Details Of Original Health Canada Recall Notice Here<a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>KME ( 10V386000 )</title>
		<link>http://www.recallnewsletter.com/kme-10v386000</link>
		<comments>http://www.recallnewsletter.com/kme-10v386000#comments</comments>
		<pubDate>Wed, 01 Sep 2010 10:00:17 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/kme-10v386000</guid>
		<description><![CDATA[Dated: AUG 26, 2010 KOVATCH MOBILE EQUIPMENT CORP. (KME) IS RECALLING CERTAIN MODEL YEAR 2007 THROUGH 2009 PREDATOR MODEL EMERGENCY VEHICLES MANUFACTURED FROM OCTOBER 15, 2007 THROUGH NOVEMBER 23, 2009, AND EQUIPPED WITH&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below will take you [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 26, 2010 KOVATCH MOBILE EQUIPMENT CORP. (KME) IS RECALLING CERTAIN MODEL YEAR 2007 THROUGH 2009 PREDATOR MODEL EMERGENCY VEHICLES MANUFACTURED FROM OCTOBER 15, 2007 THROUGH NOVEMBER 23, 2009, AND EQUIPPED WITH&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V386000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<item>
		<title>PONTIAC ( 10V387000 )</title>
		<link>http://www.recallnewsletter.com/pontiac-10v387000</link>
		<comments>http://www.recallnewsletter.com/pontiac-10v387000#comments</comments>
		<pubDate>Wed, 01 Sep 2010 10:00:09 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/pontiac-10v387000</guid>
		<description><![CDATA[Dated: AUG 26, 2010 GM IS RECALLING CERTAIN MODEL YEAR 2005-2008 PONTIAC VIBE VEHICLES. THE ENGINE CONTROL MODULE (ECM) FOR THE SUBJECT MODELS EQUIPPED WITH THE 1ZZ-FE (LV6) ENGINE AND TWO-WHEEL DRIVE MAY HAVE BEEN IMPR&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 26, 2010 GM IS RECALLING CERTAIN MODEL YEAR 2005-2008 PONTIAC VIBE VEHICLES.  THE ENGINE CONTROL MODULE (ECM) FOR THE SUBJECT MODELS EQUIPPED WITH THE 1ZZ-FE (LV6) ENGINE AND TWO-WHEEL DRIVE MAY HAVE BEEN IMPR&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V387000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<title>Torn &amp; Glasser Issues Allergy Alert on Undeclared Peanuts Fancy, No Peanuts</title>
		<link>http://www.recallnewsletter.com/torn-glasser-issues-allergy-alert-on-undeclared-peanuts-fancy-no-peanuts</link>
		<comments>http://www.recallnewsletter.com/torn-glasser-issues-allergy-alert-on-undeclared-peanuts-fancy-no-peanuts#comments</comments>
		<pubDate>Tue, 31 Aug 2010 21:00:09 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/torn-glasser-issues-allergy-alert-on-undeclared-peanuts-fancy-no-peanuts</guid>
		<description><![CDATA[Torn &#38; Glasser of Rancho Dominguez, CA is recalling its 3.75lb (#10) cans of “Mixed Nuts Fancy, No Peanuts” marked with lot numbers 0980 and 1940 on the outer case label and bottom lid due to undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Torn &amp; Glasser of Rancho Dominguez, CA is recalling its 3.75lb (#10) cans of “Mixed Nuts Fancy, No Peanuts” marked with lot numbers 0980 and 1940 on the outer case label and bottom lid due to undeclared peanuts. People who have allergies to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.<br />
The recalled “Mixed Nuts Fancy, No Peanuts” were distributed in CA, WA and HI. This was distributed through a wholesale distribution outlet. The product comes in a sealed, 3.75lb #10 style can marked with lot numbers 0980 and 1940 on the outer case label and bottom lid. The UPC is 072488980761.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224569.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>FDA seeks court order against Michigan dairy</title>
		<link>http://www.recallnewsletter.com/fda-seeks-court-order-against-michigan-dairy</link>
		<comments>http://www.recallnewsletter.com/fda-seeks-court-order-against-michigan-dairy#comments</comments>
		<pubDate>Tue, 31 Aug 2010 20:48:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/fda-seeks-court-order-against-michigan-dairy</guid>
		<description><![CDATA[The U.S. Department of Justice, on behalf of the U.S. Food and Drug Administration, has filed a complaint for permanent injunction against Scenic View Dairy of Hamilton, Mich., its president, and three of its managers alleging that they sold dairy cows for human consumption that contained illegal drug residues in edible tissues. This is a [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The U.S. Department of Justice, on behalf of the U.S. Food and Drug Administration, has filed a complaint for permanent injunction against Scenic View Dairy of Hamilton, Mich., its president, and three of its managers alleging that they sold dairy cows for human consumption that contained illegal drug residues in edible tissues.</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm224574.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>Paleta California Co. Announces Voluntary Recall of Frozen Mamey Paletas Because of Potential Contamination with Salmonella Typhi</title>
		<link>http://www.recallnewsletter.com/paleta-california-co-announces-voluntary-recall-of-frozen-mamey-paletas-because-of-potential-contamination-with-salmonella-typhi</link>
		<comments>http://www.recallnewsletter.com/paleta-california-co-announces-voluntary-recall-of-frozen-mamey-paletas-because-of-potential-contamination-with-salmonella-typhi#comments</comments>
		<pubDate>Tue, 31 Aug 2010 18:48:02 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/paleta-california-co-announces-voluntary-recall-of-frozen-mamey-paletas-because-of-potential-contamination-with-salmonella-typhi</guid>
		<description><![CDATA[In response to the voluntary recall by Goya Foods, Inc. of their frozen mamey pulp, Paleta California, Co. is voluntarily recalling its 4 oz. Mamey Supreme Cream Bar (frozen fruit bars also known as “paletas”) due to a potential health risk from Salmonella Typhi. Salmonella Typhi is a bacterium that causes a life-threatening illness called [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>In response to the voluntary recall by Goya Foods, Inc. of their frozen mamey pulp, Paleta California, Co. is voluntarily recalling its 4 oz. Mamey Supreme Cream Bar (frozen fruit bars also known as “paletas”) due to a potential health risk from Salmonella Typhi. Salmonella Typhi is a bacterium that causes a life-threatening illness called typhoid fever.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224510.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Morningland Dairy Conducting Nationwide Voluntary Recall of All Cheese Labeled as Morningland Dairy &amp; Ozark Hills Farm Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/morningland-dairy-conducting-nationwide-voluntary-recall-of-all-cheese-labeled-as-morningland-dairy-ozark-hills-farm-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/morningland-dairy-conducting-nationwide-voluntary-recall-of-all-cheese-labeled-as-morningland-dairy-ozark-hills-farm-because-of-possible-health-risk#comments</comments>
		<pubDate>Tue, 31 Aug 2010 18:48:02 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/morningland-dairy-conducting-nationwide-voluntary-recall-of-all-cheese-labeled-as-morningland-dairy-ozark-hills-farm-because-of-possible-health-risk</guid>
		<description><![CDATA[Morningland Dairy of Mountain View, Missouri, is recalling 68,957 pounds of cheese because it may be contaminated with Listeria monocytogene and also has the potential to be contaminated with Staphylococcus aureus.Morningland Dairy’s raw milk cheese is sold in the lower 48 states via mail order, retail stores, crop sharing associations, and direct delivery. The cheese [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Morningland Dairy of Mountain View, Missouri, is recalling 68,957 pounds of cheese because it may be contaminated with Listeria monocytogene and also has the potential to be contaminated with Staphylococcus aureus.Morningland Dairy’s raw milk cheese is sold in the lower 48 states via mail order, retail stores, crop sharing associations, and direct delivery.  The cheese is packaged in vacuum-sealed plastic packages that are sold as random weight size retail packages. The specific varieties of cheese are sold under the following brand names and flavors:</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224494.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Reminding Parents of School Lunch Allergen Safety</title>
		<link>http://www.recallnewsletter.com/reminding-parents-of-school-lunch-allergen-safety</link>
		<comments>http://www.recallnewsletter.com/reminding-parents-of-school-lunch-allergen-safety#comments</comments>
		<pubDate>Tue, 31 Aug 2010 17:48:05 +0000</pubDate>
		<dc:creator>Health Canada</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Health Canada Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/reminding-parents-of-school-lunch-allergen-safety</guid>
		<description><![CDATA[As children head back to the classroom, Health Canada is reminding parents of the importance of allergy awareness when packing lunches for their children. Severe allergic reactions can occur quickly and without warning, and some foods can be life-threatening to allergic children. This is a summary of a recall issued by Health Canada. The link [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>As children head back to the classroom, Health Canada is reminding parents of the importance of allergy awareness when packing lunches for their children. Severe allergic reactions can occur quickly and without warning, and some foods can be life-threatening to allergic children.</p>
<p>This is a summary of a recall issued by Health Canada.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.hc-sc.gc.ca/ahc-asc/media/advisories-avis/_2010/2010_147-eng.php" target="_blank"><br />
View Full Details Of Original Health Canada Recall Notice Here<a>.</p>
]]></content:encoded>
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		<title>FDA launches new organizational performance management system</title>
		<link>http://www.recallnewsletter.com/fda-launches-new-organizational-performance-management-system</link>
		<comments>http://www.recallnewsletter.com/fda-launches-new-organizational-performance-management-system#comments</comments>
		<pubDate>Tue, 31 Aug 2010 17:24:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/fda-launches-new-organizational-performance-management-system</guid>
		<description><![CDATA[The U.S. Food and Drug Administration today launched an innovative performance management system designed to advance the President’s commitment to transparency, public participation, and collaboration in the work of government. This is a summary of a Press Release issued by the Food and Drug Administration (FDA). The link below will take you to the original [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The U.S. Food and Drug Administration today launched an innovative performance management system designed to advance the President’s commitment to transparency, public participation, and collaboration in the work of government.</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm224401.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<title>32-Inch Sharp LCD-TVs Recalled Due to Risk of Injury</title>
		<link>http://www.recallnewsletter.com/32-inch-sharp-lcd-tvs-recalled-due-to-risk-of-injury</link>
		<comments>http://www.recallnewsletter.com/32-inch-sharp-lcd-tvs-recalled-due-to-risk-of-injury#comments</comments>
		<pubDate>Tue, 31 Aug 2010 16:24:03 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Household Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/32-inch-sharp-lcd-tvs-recalled-due-to-risk-of-injury</guid>
		<description><![CDATA[The TV stand&#8217;s neck support can break and cause the TV to tip-over, posing a risk of injury to the consumer. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original recall press release containing complete information, including instructions about what [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The TV stand&#8217;s neck support can break and cause the TV to tip-over, posing a risk of injury to the consumer.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10329.html" target="_blank">View Full Details Of Original CSPC Recall Notice Here</a></p>
]]></content:encoded>
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		<title>Slow Cookers Recalled by Sensio Due to Fire Hazard; Sold Exclusively at Kohl&#8217;s Department Stores</title>
		<link>http://www.recallnewsletter.com/slow-cookers-recalled-by-sensio-due-to-fire-hazard-sold-exclusively-at-kohls-department-stores</link>
		<comments>http://www.recallnewsletter.com/slow-cookers-recalled-by-sensio-due-to-fire-hazard-sold-exclusively-at-kohls-department-stores#comments</comments>
		<pubDate>Tue, 31 Aug 2010 14:48:13 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Household Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/slow-cookers-recalled-by-sensio-due-to-fire-hazard-sold-exclusively-at-kohls-department-stores</guid>
		<description><![CDATA[The slow cooker&#8217;s control panel can overheat and melt, posing a fire hazard. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The slow cooker&#8217;s control panel can overheat and melt, posing a fire hazard.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10328.html" target="_blank">View Full Details Of Original CSPC Recall Notice Here</a></p>
]]></content:encoded>
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		<title>P&amp;G Recalls Small Number of Bags of Cat Food From Stores in Loveland, Colorado</title>
		<link>http://www.recallnewsletter.com/pg-recalls-small-number-of-bags-of-cat-food-from-stores-in-loveland-colorado</link>
		<comments>http://www.recallnewsletter.com/pg-recalls-small-number-of-bags-of-cat-food-from-stores-in-loveland-colorado#comments</comments>
		<pubDate>Mon, 30 Aug 2010 15:56:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/pg-recalls-small-number-of-bags-of-cat-food-from-stores-in-loveland-colorado</guid>
		<description><![CDATA[CINCINNATI, August 29, 2010 &#8212; Procter &#38; Gamble (P&#38;G) is voluntarily recalling a small number of bags of its Iams Proactive Health Indoor Weight &#38; Hairball Care dry cat food which may have been sold recently in one or two stores in Loveland, Colorado. This is a summary of a recall issued by the Food [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>CINCINNATI, August 29, 2010 &#8212; Procter &amp; Gamble (P&amp;G) is voluntarily recalling a small number of bags of its Iams Proactive Health Indoor Weight &amp; Hairball Care dry cat food which may have been sold recently in one or two stores in Loveland, Colorado.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224352.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Sparboe Farms Initiated Voluntary Recall Fresh Shell Eggs</title>
		<link>http://www.recallnewsletter.com/sparboe-farms-initiated-voluntary-recall-fresh-shell-eggs</link>
		<comments>http://www.recallnewsletter.com/sparboe-farms-initiated-voluntary-recall-fresh-shell-eggs#comments</comments>
		<pubDate>Sat, 28 Aug 2010 15:48:10 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/sparboe-farms-initiated-voluntary-recall-fresh-shell-eggs</guid>
		<description><![CDATA[Sparboe Farms is voluntarily recalling shell eggs produced by Wright County Egg and Hillandale Farms which were packaged by Sparboe Farms, because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Sparboe Farms is voluntarily recalling shell eggs produced by Wright County Egg and Hillandale Farms which were packaged by Sparboe Farms, because they have the potential to be contaminated with Salmonella.  Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis, or arthritis.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224301.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>FORD ( 10V385000 )</title>
		<link>http://www.recallnewsletter.com/ford-10v385000</link>
		<comments>http://www.recallnewsletter.com/ford-10v385000#comments</comments>
		<pubDate>Sat, 28 Aug 2010 10:00:08 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/ford-10v385000</guid>
		<description><![CDATA[Dated: AUG 26, 2010 FORD IS RECALLING CERTAIN MODEL YEAR 1998-2003 WINDSTAR VEHICLES MANUFACTURED FROM SEPTEMBER 1, 1997 THROUGH FEBRUARY 28, 2003 AND CURRENTLY REGISTERED OR ORIGINALLY SOLD IN CONNECTICUT, DELAWARE, DIS&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below will take you to [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 26, 2010 FORD IS RECALLING CERTAIN MODEL YEAR 1998-2003 WINDSTAR VEHICLES MANUFACTURED FROM SEPTEMBER 1, 1997 THROUGH FEBRUARY 28, 2003 AND CURRENTLY REGISTERED OR ORIGINALLY SOLD IN CONNECTICUT, DELAWARE, DIS&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V385000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<title>Pennsylvania Firm Recalls Ground Beef Products Due to Possible E. coli O26 Contamination</title>
		<link>http://www.recallnewsletter.com/pennsylvania-firm-recalls-ground-beef-products-due-to-possible-e-coli-o26-contamination</link>
		<comments>http://www.recallnewsletter.com/pennsylvania-firm-recalls-ground-beef-products-due-to-possible-e-coli-o26-contamination#comments</comments>
		<pubDate>Sat, 28 Aug 2010 06:24:05 +0000</pubDate>
		<dc:creator>USDA FSIS</dc:creator>
				<category><![CDATA[Food Recalls]]></category>
		<category><![CDATA[USDA Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/pennsylvania-firm-recalls-ground-beef-products-due-to-possible-e-coli-o26-contamination</guid>
		<description><![CDATA[Cargill Meat Solutions Corp., a Wyalusing, Pa. establishment, is recalling approximately 8,500 pounds of ground beef products that may be contaminated with E. coli O26, the U.S. Department of Agriculture&#8217;s Food Safety and Inspection Service (FSIS) announced today. This is a summary of a recall issued by the USDA Food Safety and Inspection Service (FSIS). [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Cargill Meat Solutions Corp., a Wyalusing, Pa. establishment, is recalling approximately 8,500 pounds of ground beef products that may be contaminated with E. coli O26, the U.S. Department of Agriculture&#8217;s Food Safety and Inspection Service (FSIS) announced today.</p>
<p>This is a summary of a recall issued by the USDA Food Safety and Inspection Service (FSIS).  The link below will take you to the original recall press release, containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fsis.usda.gov/News_&amp;_Events/Recall_050_2010_Release/index.asp" target="_blank">View Full Details Of Original USDA FSIS Recall Notice Here.</a></p>
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		<title>Queseria Chipilo Recalls Cheese Products Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/queseria-chipilo-recalls-cheese-products-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/queseria-chipilo-recalls-cheese-products-because-of-possible-health-risk#comments</comments>
		<pubDate>Sat, 28 Aug 2010 02:00:07 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/queseria-chipilo-recalls-cheese-products-because-of-possible-health-risk</guid>
		<description><![CDATA[Queseria Chipilo , Passaic, NJ is announcing to recall of the following cheese products, all date codes up to and including Sept. 26, 2010 Fresco and Nov. 25,2010 Oaxaca.Oaxaca String Cheese Queso Fresco . Queso Fresco. Hoja De Plátano This is a summary of a recall issued by the Food and Drug Administration (FDA). The [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Queseria Chipilo , Passaic, NJ    is announcing to recall of the following cheese products, all date codes up to and including Sept. 26, 2010 Fresco and Nov. 25,2010 Oaxaca.Oaxaca String Cheese<br />
Queso Fresco . Queso Fresco. Hoja De Plátano</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224300.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>Fruiti Pops, Inc. Recalls &quot;Fruiti Pops&quot; Brand Mamey Frozen Fruit Bars Because of Potential Health Risk</title>
		<link>http://www.recallnewsletter.com/fruiti-pops-inc-recalls-fruiti-pops-brand-mamey-frozen-fruit-bars-because-of-potential-health-risk</link>
		<comments>http://www.recallnewsletter.com/fruiti-pops-inc-recalls-fruiti-pops-brand-mamey-frozen-fruit-bars-because-of-potential-health-risk#comments</comments>
		<pubDate>Fri, 27 Aug 2010 20:00:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/fruiti-pops-inc-recalls-fruiti-pops-brand-mamey-frozen-fruit-bars-because-of-potential-health-risk</guid>
		<description><![CDATA[In response to the voluntary recall of Goya Foods, Inc. frozen mamey pulp, Fruiti Pops, Inc. of Santa Fe Springs, CA is recalling its Fruiti Pops 4 oz. Mamey frozen fruit bars due to a potential health risk from Salmonella typhi. No illnesses have been reported to date in connection with Fruiti Pops Mamey fruit [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>In response to the voluntary recall of Goya Foods, Inc. frozen mamey pulp, Fruiti Pops, Inc. of Santa Fe Springs, CA is recalling its Fruiti Pops 4 oz. Mamey frozen fruit bars due to a potential health risk from Salmonella typhi. No illnesses have been reported to date in connection with Fruiti Pops Mamey fruit bars.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224278.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Cal-Maine Foods, Inc. Clarifies Previous Statement on Nationwide Shell Egg Recall</title>
		<link>http://www.recallnewsletter.com/cal-maine-foods-inc-clarifies-previous-statement-on-nationwide-shell-egg-recall</link>
		<comments>http://www.recallnewsletter.com/cal-maine-foods-inc-clarifies-previous-statement-on-nationwide-shell-egg-recall#comments</comments>
		<pubDate>Fri, 27 Aug 2010 14:48:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/cal-maine-foods-inc-clarifies-previous-statement-on-nationwide-shell-egg-recall</guid>
		<description><![CDATA[Cal-Maine Foods, Inc. (NASDAQ: CALM) today issued the following clarification regarding the previously announced voluntary recall of shell eggs supplied from Hillandale Farms of Iowa. This information does not increase the total number of eggs which Cal-Maine purchased from Hillandale Farms, which was previously announced on August 20, 2010. Cal-Maine immediately contacted its customers to [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Cal-Maine Foods, Inc. (NASDAQ: CALM) today issued the following clarification regarding the previously announced voluntary recall of shell eggs supplied from Hillandale Farms of Iowa.  This information does not increase the total number of eggs which Cal-Maine purchased from Hillandale Farms, which was previously announced on August 20, 2010. Cal-Maine immediately contacted its customers to ensure that any eggs included in the recall were withdrawn from the marketplace.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224199.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>TOYOTA ( 10V384000 )</title>
		<link>http://www.recallnewsletter.com/toyota-10v384000</link>
		<comments>http://www.recallnewsletter.com/toyota-10v384000#comments</comments>
		<pubDate>Fri, 27 Aug 2010 10:00:09 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/toyota-10v384000</guid>
		<description><![CDATA[Dated: AUG 26, 2010 TOYOTA IS RECALLING CERTAIN MODEL YEAR 2005-2008 COROLLA AND COROLLA MATRIX VEHICLES. THE ENGINE CONTROL MODULE (ECM) FOR THE SUBJECT MODELS EQUIPPED WITH THE 1ZZ-FE ENGINE AND TWO-WHEEL DRIVE MAY HA&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below will [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 26, 2010 TOYOTA IS RECALLING CERTAIN MODEL YEAR 2005-2008 COROLLA AND COROLLA MATRIX VEHICLES.  THE ENGINE CONTROL MODULE (ECM) FOR THE SUBJECT MODELS EQUIPPED WITH THE 1ZZ-FE ENGINE AND TWO-WHEEL DRIVE MAY HA&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V384000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		</item>
		<item>
		<title>INTERNATIONAL ( 10V383000 )</title>
		<link>http://www.recallnewsletter.com/international-10v383000</link>
		<comments>http://www.recallnewsletter.com/international-10v383000#comments</comments>
		<pubDate>Fri, 27 Aug 2010 10:00:05 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/international-10v383000</guid>
		<description><![CDATA[Dated: AUG 24, 2010 NAVISTAR IS RECALLING CERTAIN MODEL YEAR 2008 THROUGH 2011 INTERNATIONAL PROSTAR AND LONESTAR HEAVY TRUCKS MANUFACTURED FROM JANUARY 2, 2007 THROUGH JUNE 1, 2010. THE PASSENGER SIDE WINDSHIELD WIPER &#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below will take [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 24, 2010 NAVISTAR IS RECALLING CERTAIN MODEL YEAR 2008 THROUGH 2011 INTERNATIONAL PROSTAR AND LONESTAR HEAVY TRUCKS MANUFACTURED FROM JANUARY 2, 2007 THROUGH JUNE 1, 2010.  THE PASSENGER SIDE WINDSHIELD WIPER &#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V383000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
			<wfw:commentRss>http://www.recallnewsletter.com/international-10v383000/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Huber Needles: Recall &#8211; Risk of Coring</title>
		<link>http://www.recallnewsletter.com/huber-needles-recall-risk-of-coring</link>
		<comments>http://www.recallnewsletter.com/huber-needles-recall-risk-of-coring#comments</comments>
		<pubDate>Thu, 26 Aug 2010 20:00:13 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/huber-needles-recall-risk-of-coring</guid>
		<description><![CDATA[Risk of infection, damage or death of tissue, swelling, or other serious adverse health consequences occurring as a result of the core travelling through blood vessels into the patient’s lungs. This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Risk of infection, damage or death of tissue, swelling, or other serious adverse health consequences occurring as a result of the core travelling through blood vessels into the patient’s lungs.</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm224163.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Fingerstick Devices to Obtain Blood Specimens: Initial Communication &#8211; Risk of Transmitting Bloodborne Pathogens</title>
		<link>http://www.recallnewsletter.com/fingerstick-devices-to-obtain-blood-specimens-initial-communication-risk-of-transmitting-bloodborne-pathogens</link>
		<comments>http://www.recallnewsletter.com/fingerstick-devices-to-obtain-blood-specimens-initial-communication-risk-of-transmitting-bloodborne-pathogens#comments</comments>
		<pubDate>Thu, 26 Aug 2010 18:48:24 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/fingerstick-devices-to-obtain-blood-specimens-initial-communication-risk-of-transmitting-bloodborne-pathogens</guid>
		<description><![CDATA[Increase in reports of bloodborne infection transmission resulting from the shared use of fingerstick and point-of-care blood testing devices. This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice. View Full Details Of The Original MedWatch [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Increase in reports of bloodborne infection transmission resulting from the shared use of fingerstick and  point-of-care blood testing devices.</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm224135.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Parents and Caregivers Warned About the Dangers of Baby Hammocks</title>
		<link>http://www.recallnewsletter.com/parents-and-caregivers-warned-about-the-dangers-of-baby-hammocks</link>
		<comments>http://www.recallnewsletter.com/parents-and-caregivers-warned-about-the-dangers-of-baby-hammocks#comments</comments>
		<pubDate>Thu, 26 Aug 2010 18:00:15 +0000</pubDate>
		<dc:creator>Health Canada</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Health Canada Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/parents-and-caregivers-warned-about-the-dangers-of-baby-hammocks</guid>
		<description><![CDATA[Health Canada is again warning parents and caregivers against using hammocks designed for infants and young children due to the potential suffocation hazard posed by these products. The product&#8217;s inclined sleeping surface increases the risk of infants rolling and becoming wedged in a position where they can no longer breathe. This is a summary of [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Health Canada is again warning parents and caregivers against using hammocks designed for infants and young children due to the potential suffocation hazard posed by these products. The product&#8217;s inclined sleeping surface increases the risk of infants rolling and becoming wedged in a position where they can no longer breathe.</p>
<p>This is a summary of a recall issued by Health Canada.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.hc-sc.gc.ca/ahc-asc/media/advisories-avis/_2010/2010_146-eng.php" target="_blank"><br />
View Full Details Of Original Health Canada Recall Notice Here<a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Magnetic Maze Boards Recalled by Lakeshore Learning Materials Due to Choking, Intestinal and Aspiration Hazards</title>
		<link>http://www.recallnewsletter.com/magnetic-maze-boards-recalled-by-lakeshore-learning-materials-due-to-choking-intestinal-and-aspiration-hazards</link>
		<comments>http://www.recallnewsletter.com/magnetic-maze-boards-recalled-by-lakeshore-learning-materials-due-to-choking-intestinal-and-aspiration-hazards#comments</comments>
		<pubDate>Thu, 26 Aug 2010 15:24:04 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Children's Toy Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/magnetic-maze-boards-recalled-by-lakeshore-learning-materials-due-to-choking-intestinal-and-aspiration-hazards</guid>
		<description><![CDATA[The magnetic maze board&#8217;s plastic wand can separate and expose a magnet that can be a choking hazard to children. Also, if a child has more than one of these toys and the magnets detach and are swallowed, the magnets can attract each other and cause intestinal perforations or blockages, which can be fatal. This [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The magnetic maze board&#8217;s plastic wand can separate and expose a magnet that can be a choking hazard to children. Also, if a child has more than one of these toys and the magnets detach and are swallowed, the magnets can attract each other and cause intestinal perforations or blockages, which can be fatal.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10327.html" target="_blank"> View Full Details Of Original CPSC Recall Notice Here</a>, Including Pictures If Any.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Cardenas Market Brand Label Included in Wright County Egg Recall</title>
		<link>http://www.recallnewsletter.com/cardenas-market-brand-label-included-in-wright-county-egg-recall</link>
		<comments>http://www.recallnewsletter.com/cardenas-market-brand-label-included-in-wright-county-egg-recall#comments</comments>
		<pubDate>Wed, 25 Aug 2010 22:24:04 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/cardenas-market-brand-label-included-in-wright-county-egg-recall</guid>
		<description><![CDATA[The following statement was released by officials of Wright County Egg regarding its voluntary recall of some shell eggs in cooperation with the US Food and Drug Administration&#8217;s (FDA). Wright County Egg of Galt, Iowa is adding one California-distributed brand label – Cardenas Market – to its voluntary recall of August 13, 2010 of specific [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The following statement was released by officials of Wright County Egg regarding its voluntary recall of some shell eggs in cooperation with the US Food and Drug Administration&#8217;s (FDA). Wright County Egg of Galt, Iowa is adding one California-distributed brand label – Cardenas Market – to its voluntary recall of August 13, 2010 of specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella&#8230;</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224085.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Trafficanda Egg Ranch Initiates Voluntary Recall of Medium, Large, X Large, &amp; Jumbo AA Cartons; 5 Dozen Medium Over Wrap &amp; 20 Count Over Wrap, Fresh Shell Eggs Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/trafficanda-egg-ranch-initiates-voluntary-recall-of-medium-large-x-large-jumbo-aa-cartons-5-dozen-medium-over-wrap-20-count-over-wrap-fresh-shell-eggs-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/trafficanda-egg-ranch-initiates-voluntary-recall-of-medium-large-x-large-jumbo-aa-cartons-5-dozen-medium-over-wrap-20-count-over-wrap-fresh-shell-eggs-because-of-possible-health-risk#comments</comments>
		<pubDate>Wed, 25 Aug 2010 22:24:02 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/trafficanda-egg-ranch-initiates-voluntary-recall-of-medium-large-x-large-jumbo-aa-cartons-5-dozen-medium-over-wrap-20-count-over-wrap-fresh-shell-eggs-because-of-possible-health-risk</guid>
		<description><![CDATA[The following statement was released by officials of Trafficanda Egg Ranch regarding the voluntary recall of shell eggs supplied from Wright County Egg of Galt, Iowa and distributed by Trafficanda Egg Ranch. Trafficanda Egg Ranch is voluntarily recalling specific Julian dates of Medium, Large, X Large, and Jumbo Cartons; 5 Dozen Medium Over Wrap and [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The following statement was released by officials of Trafficanda Egg Ranch regarding the voluntary recall of shell eggs supplied from Wright County Egg of Galt, Iowa and distributed by Trafficanda Egg Ranch. Trafficanda Egg Ranch is voluntarily recalling specific Julian dates of Medium, Large, X Large, and Jumbo Cartons; 5 Dozen Medium Over Wrap and 20 Count Over Wrap of shell eggs produced by Wright County Egg of Galt, Iowa because they have the potential to be contaminated with Salmonella&#8230;</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm224076.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>TimeOut Capsules: Undeclared Drug Ingredient</title>
		<link>http://www.recallnewsletter.com/timeout-capsules-undeclared-drug-ingredient</link>
		<comments>http://www.recallnewsletter.com/timeout-capsules-undeclared-drug-ingredient#comments</comments>
		<pubDate>Wed, 25 Aug 2010 19:48:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/timeout-capsules-undeclared-drug-ingredient</guid>
		<description><![CDATA[Product marketed as dietary supplement contains undeclared hydroxythiohomosildenafil, a chemical similar to sildenafil, which may interact with nitrates found in some prescription drugs and lower blood pressure to dangerous levels. This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Product marketed as dietary supplement contains undeclared hydroxythiohomosildenafil, a chemical similar to sildenafil, which may interact with nitrates found in some prescription drugs and lower blood pressure to dangerous levels.</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm224073.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>FDA Warns Consumers to Avoid TimeOut Capsules</title>
		<link>http://www.recallnewsletter.com/fda-warns-consumers-to-avoid-timeout-capsules</link>
		<comments>http://www.recallnewsletter.com/fda-warns-consumers-to-avoid-timeout-capsules#comments</comments>
		<pubDate>Wed, 25 Aug 2010 19:00:10 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/fda-warns-consumers-to-avoid-timeout-capsules</guid>
		<description><![CDATA[The U.S. Food and Drug Administration is warning consumers not to take TimeOut Capsules because it contains an active drug ingredient that can dangerously lower blood pressure. The product is marketed as a dietary supplement for sexual enhancement. This is a summary of a Press Release issued by the Food and Drug Administration (FDA). The [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The U.S. Food and Drug Administration is warning consumers not to take TimeOut Capsules because it contains an active drug ingredient that can dangerously lower blood pressure. The product is marketed as a dietary supplement for sexual enhancement.</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm224065.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Important Diabetes Information: GlucaGen Hypokit being Recalled in Canada</title>
		<link>http://www.recallnewsletter.com/important-diabetes-information-glucagen-hypokit-being-recalled-in-canada</link>
		<comments>http://www.recallnewsletter.com/important-diabetes-information-glucagen-hypokit-being-recalled-in-canada#comments</comments>
		<pubDate>Wed, 25 Aug 2010 16:24:08 +0000</pubDate>
		<dc:creator>Health Canada</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Health Canada Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/important-diabetes-information-glucagen-hypokit-being-recalled-in-canada</guid>
		<description><![CDATA[Health Canada is informing Canadians that Novo Nordisk Canada Inc. has agreed to voluntarily recall two lots (YW60335 and YW60351) of their product, GlucaGen Hypokit (DIN 02333627) currently available on the Canadian market. This is a summary of a recall issued by Health Canada. The link below will take you to the original recall press [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Health Canada is informing Canadians that Novo Nordisk Canada Inc. has agreed to voluntarily recall two lots (YW60335 and YW60351) of their product, GlucaGen Hypokit (DIN 02333627) currently available on the Canadian market.</p>
<p>This is a summary of a recall issued by Health Canada.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.hc-sc.gc.ca/ahc-asc/media/advisories-avis/_2010/2010_145-eng.php" target="_blank"><br />
View Full Details Of Original Health Canada Recall Notice Here<a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Octagam [Immune Globulin Intravenous (human)] 5&#037; Liquid Preparation: Market Withdrawal &#8211; Risk of Thromboembolic Events</title>
		<link>http://www.recallnewsletter.com/octagam-immune-globulin-intravenous-human-5-liquid-preparation-market-withdrawal-risk-of-thromboembolic-events</link>
		<comments>http://www.recallnewsletter.com/octagam-immune-globulin-intravenous-human-5-liquid-preparation-market-withdrawal-risk-of-thromboembolic-events#comments</comments>
		<pubDate>Wed, 25 Aug 2010 15:48:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/octagam-immune-globulin-intravenous-human-5-liquid-preparation-market-withdrawal-risk-of-thromboembolic-events</guid>
		<description><![CDATA[Customers asked to immediately quarantine the use of affected lots due to the potential for serious thromboembolic events. This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice. View Full Details Of The Original MedWatch Notice [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Customers asked to immediately quarantine the use of affected lots  due to the potential for serious thromboembolic events.</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm223968.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Octagam [Immune Globulin Intravenous (human)] 5&#037; Liquid Preparation: Recall &#8211; Risk of Thromboembolic Events</title>
		<link>http://www.recallnewsletter.com/octagam-immune-globulin-intravenous-human-5-liquid-preparation-recall-risk-of-thromboembolic-events</link>
		<comments>http://www.recallnewsletter.com/octagam-immune-globulin-intravenous-human-5-liquid-preparation-recall-risk-of-thromboembolic-events#comments</comments>
		<pubDate>Wed, 25 Aug 2010 15:24:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/octagam-immune-globulin-intravenous-human-5-liquid-preparation-recall-risk-of-thromboembolic-events</guid>
		<description><![CDATA[Customers asked to immediately quarantine the use of affected lots due to the potential for serious thromboembolic events. This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice. View Full Details Of The Original MedWatch Notice [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Customers asked to immediately quarantine the use of affected lots  due to the potential for serious thromboembolic events.</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm223968.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Television Wall Mounts Recalled by Milestone AV Technologies Due to Injury Hazard</title>
		<link>http://www.recallnewsletter.com/television-wall-mounts-recalled-by-milestone-av-technologies-due-to-injury-hazard</link>
		<comments>http://www.recallnewsletter.com/television-wall-mounts-recalled-by-milestone-av-technologies-due-to-injury-hazard#comments</comments>
		<pubDate>Wed, 25 Aug 2010 15:24:03 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Household Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/television-wall-mounts-recalled-by-milestone-av-technologies-due-to-injury-hazard</guid>
		<description><![CDATA[The elbow joint components on the wall mount&#8217;s arm do not fit together properly, causing the attached television to tilt and possibly fall when the television is adjusted. This could pose an injury hazard to a consumer. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The elbow joint components on the wall mount&#8217;s arm do not fit together properly, causing the attached television to tilt and possibly fall when the television is adjusted. This could pose an injury hazard to a consumer.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10326.html" target="_blank">View Full Details Of Original CSPC Recall Notice Here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://www.recallnewsletter.com/television-wall-mounts-recalled-by-milestone-av-technologies-due-to-injury-hazard/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
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		<title>Azteca Linda Corp.  Recalls Queso Fresco and Queso Hebra because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/azteca-linda-corp-recalls-queso-fresco-and-queso-hebra-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/azteca-linda-corp-recalls-queso-fresco-and-queso-hebra-because-of-possible-health-risk#comments</comments>
		<pubDate>Wed, 25 Aug 2010 14:00:04 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/azteca-linda-corp-recalls-queso-fresco-and-queso-hebra-because-of-possible-health-risk</guid>
		<description><![CDATA[Azteca Linda Corp. of Brooklyn, NY, is recalling QUESO FRESCO (FRESH WHITE CHEESE) and QUESO HEBRA (FRESH WHITE STRING CHEESE) with an expiration date of September 11, 2010 because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Azteca Linda Corp. of Brooklyn, NY, is recalling QUESO FRESCO (FRESH WHITE CHEESE) and QUESO HEBRA (FRESH WHITE STRING CHEESE) with an expiration date of September 11, 2010 because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223977.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>HEALTH HAZARD ALERT &#8211; Certain LA NUESTRA brand FROZEN MAMEY PULP may contain Salmonella bacteria</title>
		<link>http://www.recallnewsletter.com/health-hazard-alert-certain-la-nuestra-brand-frozen-mamey-pulp-may-contain-salmonella-bacteria</link>
		<comments>http://www.recallnewsletter.com/health-hazard-alert-certain-la-nuestra-brand-frozen-mamey-pulp-may-contain-salmonella-bacteria#comments</comments>
		<pubDate>Wed, 25 Aug 2010 08:48:07 +0000</pubDate>
		<dc:creator>CFIA</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Food Recalls Canada CFIA]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/health-hazard-alert-certain-la-nuestra-brand-frozen-mamey-pulp-may-contain-salmonella-bacteria</guid>
		<description><![CDATA[The Canadian Food Inspection Agency (CFIA) is warning consumers not to consume La Nuestra Mamey Pulp as it may be contaminated with Salmonella. This is a summary of a recall issued by the Canadian Food Inspection Agency. The link below will take you to the original recall press release containing complete information, including instructions about [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The Canadian Food Inspection Agency (CFIA) is warning consumers not to consume La Nuestra Mamey Pulp as it may be contaminated with Salmonella.</p>
<p>This is a summary of a recall issued by the Canadian Food Inspection Agency.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://inspection.gc.ca/english/corpaffr/recarapp/2010/20100824e.shtml" target="_blank">View Full Details Of Original CFIA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Natural Wellness, Inc. Issues a Nationwide Voluntary Recall of Masxtreme Capsules, Marketed as a Dietary Supplement &#8211; 08/24/10</title>
		<link>http://www.recallnewsletter.com/natural-wellness-inc-issues-a-nationwide-voluntary-recall-of-masxtreme-capsules-marketed-as-a-dietary-supplement-082410</link>
		<comments>http://www.recallnewsletter.com/natural-wellness-inc-issues-a-nationwide-voluntary-recall-of-masxtreme-capsules-marketed-as-a-dietary-supplement-082410#comments</comments>
		<pubDate>Tue, 24 Aug 2010 21:24:02 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/natural-wellness-inc-issues-a-nationwide-voluntary-recall-of-masxtreme-capsules-marketed-as-a-dietary-supplement-082410</guid>
		<description><![CDATA[Natural Wellness is announcing that it is conducting a nationwide voluntary recall of MasXtreme, Lot # 907043, UPC 094922300805. Laboratory analysis conducted by FDA has determined the product contains undeclared amounts of Aminotadalafil, an analog of tadalafil&#8230; This is a summary of a recall issued by the Food and Drug Administration (FDA). The link below will [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Natural Wellness is announcing that it is conducting a nationwide voluntary recall of MasXtreme, Lot # 907043, UPC 094922300805. Laboratory analysis conducted by FDA has determined the product contains undeclared amounts of Aminotadalafil, an analog of tadalafil&#8230;</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223937.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>FDA releases guidance on federal menu labeling requirements</title>
		<link>http://www.recallnewsletter.com/fda-releases-guidance-on-federal-menu-labeling-requirements</link>
		<comments>http://www.recallnewsletter.com/fda-releases-guidance-on-federal-menu-labeling-requirements#comments</comments>
		<pubDate>Tue, 24 Aug 2010 18:24:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/fda-releases-guidance-on-federal-menu-labeling-requirements</guid>
		<description><![CDATA[The U.S. Food and Drug Administration today released two documents that outline steps to help chain restaurants comply with new federal nutrition labeling requirements. This is a summary of a Press Release issued by the Food and Drug Administration (FDA). The link below will take you to the original press release containing complete information, including [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The U.S. Food and Drug Administration today released two documents that outline steps to help chain restaurants comply with new federal nutrition labeling requirements.</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm223880.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>FDA Warns of Possible Dangers from Portable Foot-Tanning Device</title>
		<link>http://www.recallnewsletter.com/fda-warns-of-possible-dangers-from-portable-foot-tanning-device</link>
		<comments>http://www.recallnewsletter.com/fda-warns-of-possible-dangers-from-portable-foot-tanning-device#comments</comments>
		<pubDate>Tue, 24 Aug 2010 17:00:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/fda-warns-of-possible-dangers-from-portable-foot-tanning-device</guid>
		<description><![CDATA[The U.S. Food and Drug Administration is warning consumers about the risk of ultraviolet radiation overdose with the Tootsie Tanner portable foot tanning device. This is a summary of a Press Release issued by the Food and Drug Administration (FDA). The link below will take you to the original press release containing complete information, including [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The U.S. Food and Drug Administration is warning consumers about the risk of ultraviolet radiation overdose with the Tootsie Tanner portable foot tanning device.</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm223860.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Mr. Magic Male Enhancer: Undeclared Drug Ingredient</title>
		<link>http://www.recallnewsletter.com/mr-magic-male-enhancer-undeclared-drug-ingredient</link>
		<comments>http://www.recallnewsletter.com/mr-magic-male-enhancer-undeclared-drug-ingredient#comments</comments>
		<pubDate>Tue, 24 Aug 2010 15:48:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/mr-magic-male-enhancer-undeclared-drug-ingredient</guid>
		<description><![CDATA[Product marketed as dietary supplement contains undeclared hydroxythiohomosildenafil and sulfoaildenafil, which may interact with nitrates found in some prescription drugs and lower blood pressure to dangerous levels. This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Product marketed as dietary supplement contains undeclared hydroxythiohomosildenafil and sulfoaildenafil, which may interact with nitrates found in some prescription drugs and lower blood pressure to dangerous levels.</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm223837.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Char-Broil Recalls Vertical Gas Smokers Due to Injury Hazard</title>
		<link>http://www.recallnewsletter.com/char-broil-recalls-vertical-gas-smokers-due-to-injury-hazard</link>
		<comments>http://www.recallnewsletter.com/char-broil-recalls-vertical-gas-smokers-due-to-injury-hazard#comments</comments>
		<pubDate>Tue, 24 Aug 2010 15:24:05 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Outdoor Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/char-broil-recalls-vertical-gas-smokers-due-to-injury-hazard</guid>
		<description><![CDATA[When the temperature setting is in &#8220;low,&#8221; the smoker&#8217;s hose/valve/regulator (HVR) assembly does not allow sufficient gas to flow, causing the flame to extinguish. Gas continues to flow and build up inside the smoker. If the smoker is reignited the build-up of propane gas can cause an explosion that bursts the smoker&#8217;s door open, posing [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>When the temperature setting is in &#8220;low,&#8221; the smoker&#8217;s hose/valve/regulator (HVR) assembly does not allow sufficient gas to flow, causing the flame to extinguish. Gas continues to flow and build up inside the smoker. If the smoker is reignited the build-up of propane gas can cause an explosion that bursts the smoker&#8217;s door open, posing an injury hazard.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10325.html" target="_blank">View Full Details Of Original CSPC Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Integra Issues URGENT Worldwide Recall of NeuroBalloonTM Catheter</title>
		<link>http://www.recallnewsletter.com/integra-issues-urgent-worldwide-recall-of-neuroballoontm-catheter</link>
		<comments>http://www.recallnewsletter.com/integra-issues-urgent-worldwide-recall-of-neuroballoontm-catheter#comments</comments>
		<pubDate>Tue, 24 Aug 2010 14:48:03 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/integra-issues-urgent-worldwide-recall-of-neuroballoontm-catheter</guid>
		<description><![CDATA[Integra LifeSciences Corporation, Plainsboro, New Jersey, has initiated a worldwide recall of the NeuroBalloon Catheter. There were a total of 1,924 units distributed, 258 in the United States of America 1,586 in the European Union and 80 in countries. A total of eight (8) complaints regarding the inflation or deflation of the NeuroBalloon Catheter were [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Integra LifeSciences Corporation, Plainsboro, New Jersey, has initiated a worldwide recall of the NeuroBalloon Catheter. There were a total of 1,924 units distributed, 258 in the United States of America 1,586 in the European Union and 80 in countries. A total of eight (8) complaints regarding the inflation or deflation of the NeuroBalloon Catheter were received by Integra. All complaints occurred outside the United States. No patient injuries have been reported.  As a result of the investigation performed by Integra, it was determined that this condition could exist during pre-implant testing or during the procedure.  Integra issued a voluntary recall of the affected lots of the NeuroBalloon Catheter on July 2, 2010.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223824.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<item>
		<title>Baby Hammock Metal Stands Recalled by MamaLittleHelper Due to Fall Hazard</title>
		<link>http://www.recallnewsletter.com/baby-hammock-metal-stands-recalled-by-mamalittlehelper-due-to-fall-hazard</link>
		<comments>http://www.recallnewsletter.com/baby-hammock-metal-stands-recalled-by-mamalittlehelper-due-to-fall-hazard#comments</comments>
		<pubDate>Tue, 24 Aug 2010 14:24:02 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Children's Toy Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/baby-hammock-metal-stands-recalled-by-mamalittlehelper-due-to-fall-hazard</guid>
		<description><![CDATA[The C-shaped metal stand can break where the curved arm attaches to the leg of the metal frame, posing a fall hazard to an infant in the hammock. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original recall press release [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The C-shaped metal stand can break where the curved arm attaches to the leg of the metal frame, posing a fall hazard to an infant in the hammock.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10754.html" target="_blank"> View Full Details Of Original CPSC Recall Notice Here</a>, Including Pictures If Any.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Baby Hammocks Recalled by MamaLittleHelper Due to Suffocation Hazard</title>
		<link>http://www.recallnewsletter.com/baby-hammocks-recalled-by-mamalittlehelper-due-to-suffocation-hazard</link>
		<comments>http://www.recallnewsletter.com/baby-hammocks-recalled-by-mamalittlehelper-due-to-suffocation-hazard#comments</comments>
		<pubDate>Tue, 24 Aug 2010 14:24:02 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Children's Toy Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/baby-hammocks-recalled-by-mamalittlehelper-due-to-suffocation-hazard</guid>
		<description><![CDATA[The side-to-side shifting or tilting of the hammock can cause the infant to roll and become entrapped or wedged against the hammock&#8217;s fabric and/or mattress pad, resulting in a suffocation hazard. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The side-to-side shifting or tilting of the hammock can cause the infant to roll and become entrapped or wedged against the hammock&#8217;s fabric and/or mattress pad, resulting in a suffocation hazard.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10324.html" target="_blank"> View Full Details Of Original CPSC Recall Notice Here</a>, Including Pictures If Any.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>NuCal Foods Conducts Recall of Shell Eggs Supplied from Hillandale Farms of Iowa Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/nucal-foods-conducts-recall-of-shell-eggs-supplied-from-hillandale-farms-of-iowa-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/nucal-foods-conducts-recall-of-shell-eggs-supplied-from-hillandale-farms-of-iowa-because-of-possible-health-risk#comments</comments>
		<pubDate>Tue, 24 Aug 2010 13:48:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/nucal-foods-conducts-recall-of-shell-eggs-supplied-from-hillandale-farms-of-iowa-because-of-possible-health-risk</guid>
		<description><![CDATA[RIPON, CALIFORNIA (August 20, 2010) &#8212; The following statement was released by officials of NuCal Foods of Ripon, California regarding the voluntary recall of shell eggs supplied from Hillandale Farms of Iowa. NuCal Foods is voluntarily recalling specific Julian dates of shell eggs produced by Hillandale Farms of Iowa and packaged by NuCal Foods because [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>RIPON, CALIFORNIA (August 20, 2010) &#8212; The following statement was released by officials of NuCal Foods of Ripon, California regarding the voluntary recall of shell eggs supplied from Hillandale Farms of Iowa.</p>
<p>NuCal Foods is voluntarily recalling specific Julian dates of shell eggs produced by Hillandale Farms of Iowa and packaged by NuCal Foods because they have the potential to be contaminated with Salmonella.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223760.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Moark, LLC, of Fontana, California, Recalls Shell Eggs Supplied From Hillandale Farms of Iowa Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/moark-llc-of-fontana-california-recalls-shell-eggs-supplied-from-hillandale-farms-of-iowa-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/moark-llc-of-fontana-california-recalls-shell-eggs-supplied-from-hillandale-farms-of-iowa-because-of-possible-health-risk#comments</comments>
		<pubDate>Tue, 24 Aug 2010 13:48:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/moark-llc-of-fontana-california-recalls-shell-eggs-supplied-from-hillandale-farms-of-iowa-because-of-possible-health-risk</guid>
		<description><![CDATA[Moark, LLC, is voluntarily recalling specific lots of shell eggs produced by Hillandale Farms of Iowa and packaged by Moark, LLC, because they have the potential to be contaminated with Salmonella. Potentially affected eggs that were received by Moark total approximately 24,300 dozen. Moark repackaged the eggs for retail customers (under the brand names Albertsons, [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Moark, LLC, is voluntarily recalling specific lots of shell eggs produced by Hillandale Farms of Iowa and packaged by Moark, LLC, because they have the potential to be contaminated with Salmonella. </p>
<p>Potentially affected eggs that were received by Moark total approximately 24,300 dozen.  Moark repackaged the eggs for retail customers (under the brand names Albertsons, Yucaipa Valley, Farmer’s Gems and Mountain Dairy), as well as providing unbranded eggs to foodservice customers.  The eggs were sold by Moark to retail and wholesale customers in Southern California and Las Vegas, Nevada.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223747.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
			<wfw:commentRss>http://www.recallnewsletter.com/moark-llc-of-fontana-california-recalls-shell-eggs-supplied-from-hillandale-farms-of-iowa-because-of-possible-health-risk/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
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		<title>Williams-Sonoma Recalls Baby Bottle Warmers Due to Burn Hazard</title>
		<link>http://www.recallnewsletter.com/williams-sonoma-recalls-baby-bottle-warmers-due-to-burn-hazard</link>
		<comments>http://www.recallnewsletter.com/williams-sonoma-recalls-baby-bottle-warmers-due-to-burn-hazard#comments</comments>
		<pubDate>Tue, 24 Aug 2010 13:24:04 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Children's Toy Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/williams-sonoma-recalls-baby-bottle-warmers-due-to-burn-hazard</guid>
		<description><![CDATA[The bottle warmers can overheat liquids and baby food, posing a burn hazard to adults and babies. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original recall press release containing complete information, including instructions about what to do if you [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The bottle warmers can overheat liquids and baby food, posing a burn hazard to adults and babies.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10323.html" target="_blank"> View Full Details Of Original CPSC Recall Notice Here</a>, Including Pictures If Any.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>CLUB CAR ( 10V378000 )</title>
		<link>http://www.recallnewsletter.com/club-car-10v378000</link>
		<comments>http://www.recallnewsletter.com/club-car-10v378000#comments</comments>
		<pubDate>Tue, 24 Aug 2010 10:24:04 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/club-car-10v378000</guid>
		<description><![CDATA[Dated: AUG 13, 2010 CLUB CAR IS RECALLING CERTAIN MODEL YEAR 2010 VILLAGER 2+2 LVS PASSENGER VEHICLES MANUFACTURED FROM APRIL 14 THROUGH JULY 18, 2010. THE PEDAL MAY BE MISSING A CRITICAL LOAD BEARING WELD BETWEEN THE B&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 13, 2010 CLUB CAR IS RECALLING CERTAIN MODEL YEAR 2010 VILLAGER 2+2 LVS PASSENGER VEHICLES MANUFACTURED FROM APRIL 14 THROUGH JULY 18, 2010.  THE PEDAL MAY BE MISSING A CRITICAL LOAD BEARING WELD BETWEEN THE B&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V378000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>HEALTH HAZARD ALERT &#8211; Certain MR GOUDAS brand Tahini may contain Salmonella bacteria</title>
		<link>http://www.recallnewsletter.com/health-hazard-alert-certain-mr-goudas-brand-tahini-may-contain-salmonella-bacteria</link>
		<comments>http://www.recallnewsletter.com/health-hazard-alert-certain-mr-goudas-brand-tahini-may-contain-salmonella-bacteria#comments</comments>
		<pubDate>Tue, 24 Aug 2010 03:48:06 +0000</pubDate>
		<dc:creator>CFIA</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Food Recalls Canada CFIA]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/health-hazard-alert-certain-mr-goudas-brand-tahini-may-contain-salmonella-bacteria</guid>
		<description><![CDATA[The CFIA and Goudas Food Products Co. Ltd. are warning the public not to consume the Mr Goudas brand Tahini. This is a summary of a recall issued by the Canadian Food Inspection Agency. The link below will take you to the original recall press release containing complete information, including instructions about what to do [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The CFIA and Goudas Food Products Co. Ltd. are warning the public not to consume the Mr Goudas brand Tahini.</p>
<p>This is a summary of a recall issued by the Canadian Food Inspection Agency.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.inspection.gc.ca/english/corpaffr/recarapp/2010/20100823e.shtml" target="_blank">View Full Details Of Original CFIA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>New York Firm Recalls Deli Meat Products for Possible Listeria Contamination</title>
		<link>http://www.recallnewsletter.com/new-york-firm-recalls-deli-meat-products-for-possible-listeria-contamination</link>
		<comments>http://www.recallnewsletter.com/new-york-firm-recalls-deli-meat-products-for-possible-listeria-contamination#comments</comments>
		<pubDate>Tue, 24 Aug 2010 02:24:04 +0000</pubDate>
		<dc:creator>USDA FSIS</dc:creator>
				<category><![CDATA[Food Recalls]]></category>
		<category><![CDATA[USDA Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/new-york-firm-recalls-deli-meat-products-for-possible-listeria-contamination</guid>
		<description><![CDATA[Zemco Industries, a Buffalo, N.Y., establishment, is recalling approximately 380,000 pounds of deli meat products that may be contaminated with Listeria monocytogenes. These products were distributed to delicatessens where they were further processed into sandwiches. This is a summary of a recall issued by the USDA Food Safety and Inspection Service (FSIS). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Zemco Industries, a Buffalo, N.Y., establishment, is recalling approximately 380,000 pounds of deli meat products that may be contaminated with Listeria monocytogenes. These products were distributed to delicatessens where they were further processed into sandwiches.</p>
<p>This is a summary of a recall issued by the USDA Food Safety and Inspection Service (FSIS).  The link below will take you to the original recall press release, containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fsis.usda.gov/News_&amp;_Events/Recall_049_2010_Release/index.asp" target="_blank">View Full Details Of Original USDA FSIS Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>INOMAX DS Drug-Delivery System: Class I Recall &#8211; Risk of Interruption of Drug Flow</title>
		<link>http://www.recallnewsletter.com/inomax-ds-drug-delivery-system-class-i-recall-risk-of-interruption-of-drug-flow</link>
		<comments>http://www.recallnewsletter.com/inomax-ds-drug-delivery-system-class-i-recall-risk-of-interruption-of-drug-flow#comments</comments>
		<pubDate>Tue, 24 Aug 2010 01:24:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/inomax-ds-drug-delivery-system-class-i-recall-risk-of-interruption-of-drug-flow</guid>
		<description><![CDATA[Potential for failure of a pressure switch, which may have an impact on the administration of INOMAX for inhalation to patients. This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice. View Full Details Of The [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Potential for failure of a pressure switch, which may have an impact on the administration of INOMAX for inhalation to patients.</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm223746.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>NY Fish Inc Issues an alert on uneviscerated fish</title>
		<link>http://www.recallnewsletter.com/ny-fish-inc-issues-an-alert-on-uneviscerated-fish</link>
		<comments>http://www.recallnewsletter.com/ny-fish-inc-issues-an-alert-on-uneviscerated-fish#comments</comments>
		<pubDate>Mon, 23 Aug 2010 20:48:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/ny-fish-inc-issues-an-alert-on-uneviscerated-fish</guid>
		<description><![CDATA[NY Fish Inc, 738 Chester St, Brooklyn, NY, 11236 is recalling NY Fish Brand (cold) Smoked Herring, with a code of 141, discovered by New York State Department of Agriculture and Markets Food Inspectors during a routine inspection. The product was found to be uneviscerated prior to processing. This is a summary of a recall [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>NY Fish Inc, 738 Chester St, Brooklyn, NY, 11236 is recalling NY Fish Brand (cold) Smoked Herring, with a code of 141, discovered by New York State Department of Agriculture and Markets Food Inspectors during a routine inspection. The product was found to be uneviscerated prior to processing.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223727.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
			<wfw:commentRss>http://www.recallnewsletter.com/ny-fish-inc-issues-an-alert-on-uneviscerated-fish/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
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		<title>Study: Presence of murine leukemia virus found in CFS Patients, others</title>
		<link>http://www.recallnewsletter.com/study-presence-of-murine-leukemia-virus-found-in-cfs-patients-others</link>
		<comments>http://www.recallnewsletter.com/study-presence-of-murine-leukemia-virus-found-in-cfs-patients-others#comments</comments>
		<pubDate>Mon, 23 Aug 2010 19:24:08 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/study-presence-of-murine-leukemia-virus-found-in-cfs-patients-others</guid>
		<description><![CDATA[Researchers have found murine leukemia viruses (MLV) in blood samples collected from patients diagnosed with chronic fatigue syndrome (CFS) and some healthy blood donors, according to a study published online today by the scientific journal Proceedings of the National Academy of Sciences (PNAS). This is a summary of a Press Release issued by the Food [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Researchers have found murine leukemia viruses (MLV) in blood samples collected from  patients diagnosed with chronic fatigue syndrome (CFS) and some healthy blood donors, according to a study published online today by the scientific journal Proceedings of the National Academy of Sciences (PNAS).</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm223277.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>Lubersk i Inc., Initiates Voluntary Recall of Large Fresh Shell Eggs Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/lubersk-i-inc-initiates-voluntary-recall-of-large-fresh-shell-eggs-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/lubersk-i-inc-initiates-voluntary-recall-of-large-fresh-shell-eggs-because-of-possible-health-risk#comments</comments>
		<pubDate>Sat, 21 Aug 2010 19:24:02 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/lubersk-i-inc-initiates-voluntary-recall-of-large-fresh-shell-eggs-because-of-possible-health-risk</guid>
		<description><![CDATA[The following statement was released by officials of Luberski Inc. regarding the voluntary recall of shell eggs supplied from Wright County Egg of Galt, Iowa. Luberski Inc. is voluntarily recalling specific Julian dates of shell eggs produced by Wright County Egg of Galt, Iowa because they have the potential to be contaminated with Salmonella. This [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The following statement was released by officials of Luberski Inc. regarding the voluntary recall of shell eggs supplied from Wright County Egg of Galt, Iowa.<br />
Luberski Inc. is voluntarily recalling specific Julian dates of shell eggs produced by Wright County Egg of Galt, Iowa because they have the potential to be contaminated with Salmonella.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223549.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>JAG MOBILE SOLUTIONS ( 10V381000 )</title>
		<link>http://www.recallnewsletter.com/jag-mobile-solutions-10v381000</link>
		<comments>http://www.recallnewsletter.com/jag-mobile-solutions-10v381000#comments</comments>
		<pubDate>Sat, 21 Aug 2010 10:00:07 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/jag-mobile-solutions-10v381000</guid>
		<description><![CDATA[Dated: AUG 10, 2010 JAG MOBILE SOLUTIONS IS RECALLING CERTAIN MODEL YEAR 2006 THROUGH 2011 PORTA-LISA AND PORTA-LISA PLUS MOBILE RESTROOMS, SHOWERS, AND COMBINATIONS TOWABLE TRAILERS. THE HITCH ASSEMBLY OF THE CHASSIS M&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below will take you [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 10, 2010 JAG MOBILE SOLUTIONS IS RECALLING CERTAIN MODEL YEAR 2006 THROUGH 2011 PORTA-LISA AND PORTA-LISA PLUS MOBILE RESTROOMS, SHOWERS, AND COMBINATIONS TOWABLE TRAILERS.  THE HITCH ASSEMBLY OF THE CHASSIS M&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V381000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>BLUE BIRD ( 10V380000 )</title>
		<link>http://www.recallnewsletter.com/blue-bird-10v380000</link>
		<comments>http://www.recallnewsletter.com/blue-bird-10v380000#comments</comments>
		<pubDate>Sat, 21 Aug 2010 10:00:06 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/blue-bird-10v380000</guid>
		<description><![CDATA[Dated: AUG 18, 2010 BLUE BIRD IS RECALLING CERTAIN MODEL YEAR 2007 THROUGH 2010 ALL AMERICAN NON SCHOOL BUSES MANUFACTURED FROM JULY 16, 2006 THROUGH AUGUST 3, 2010 EQUIPPED WITH CUMMINS ISB-02, ISB-07, AND ISB-10 ENGINE&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 18, 2010 BLUE BIRD IS RECALLING CERTAIN MODEL YEAR 2007 THROUGH 2010 ALL AMERICAN NON SCHOOL BUSES MANUFACTURED FROM JULY 16, 2006 THROUGH AUGUST 3, 2010 EQUIPPED WITH CUMMINS ISB-02, ISB-07, AND ISB-10 ENGINE&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V380000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>BLUE BIRD ( 10V379000 )</title>
		<link>http://www.recallnewsletter.com/blue-bird-10v379000</link>
		<comments>http://www.recallnewsletter.com/blue-bird-10v379000#comments</comments>
		<pubDate>Sat, 21 Aug 2010 10:00:05 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/blue-bird-10v379000</guid>
		<description><![CDATA[Dated: AUG 18, 2010 BLUE BIRD IS RECALLING CERTAIN MODEL YEAR 2007 THROUGH 2010 ALL AMERICAN SCHOOL BUSES MANUFACTURED FROM MAY 29, 2006 THROUGH AUGUST 7, 2010 EQUIPPED WITH CUMMINS ISB-02, ISB-07, AND ISB-10 ENGINES. A&#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 18, 2010 BLUE BIRD IS RECALLING CERTAIN MODEL YEAR 2007 THROUGH 2010 ALL AMERICAN SCHOOL BUSES MANUFACTURED FROM MAY 29, 2006 THROUGH AUGUST 7, 2010 EQUIPPED WITH CUMMINS ISB-02, ISB-07, AND ISB-10 ENGINES.  A&#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V379000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Milton&#8217;s Baking Voluntarily Recalls 24 oz. Multi-Grain Bread in Three States For Undeclared Milk in Some Loaves</title>
		<link>http://www.recallnewsletter.com/miltons-baking-voluntarily-recalls-24-oz-multi-grain-bread-in-three-states-for-undeclared-milk-in-some-loaves</link>
		<comments>http://www.recallnewsletter.com/miltons-baking-voluntarily-recalls-24-oz-multi-grain-bread-in-three-states-for-undeclared-milk-in-some-loaves#comments</comments>
		<pubDate>Fri, 20 Aug 2010 22:24:02 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/miltons-baking-voluntarily-recalls-24-oz-multi-grain-bread-in-three-states-for-undeclared-milk-in-some-loaves</guid>
		<description><![CDATA[Milton&#8217;s Baking Company is voluntarily recalling Milton&#8217;s Multi-Grain Bread which was distributed to locations in Northern and Central California, Arizona and Nevada. The company took the precautionary step because the loaves contain milk, an undeclared allergen, which may pose a potential serious and life-threatening health risk to milk-allergic individuals. This is a summary of a [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Milton&#8217;s Baking Company is voluntarily recalling Milton&#8217;s Multi-Grain Bread which was distributed to locations in Northern and Central California, Arizona and Nevada.  The company took the precautionary step because the loaves contain milk, an undeclared allergen, which may pose a potential serious and life-threatening health risk to milk-allergic individuals.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223539.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>GloryBee Foods Recalls Whole Raw Pistachio and Whole Raw Pistachio Kernels Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/glorybee-foods-recalls-whole-raw-pistachio-and-whole-raw-pistachio-kernels-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/glorybee-foods-recalls-whole-raw-pistachio-and-whole-raw-pistachio-kernels-because-of-possible-health-risk#comments</comments>
		<pubDate>Fri, 20 Aug 2010 21:24:03 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/glorybee-foods-recalls-whole-raw-pistachio-and-whole-raw-pistachio-kernels-because-of-possible-health-risk</guid>
		<description><![CDATA[GloryBee Foods, Inc., of Eugene, Oregon is voluntarily recalling Aunt Patty&#8217;s brand 5 pound bags of Whole Raw Pistachios and 25 lb. boxes of Specialty Commodities brand Whole Raw Pistachios Kernels, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>GloryBee Foods, Inc., of Eugene, Oregon is voluntarily recalling Aunt Patty&#8217;s brand 5 pound bags of Whole Raw Pistachios and 25 lb. boxes of Specialty Commodities brand Whole Raw Pistachios Kernels, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223531.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Austinuts Wholesale, Inc. Announces Voluntary Recall of Pistachio Kernel Products</title>
		<link>http://www.recallnewsletter.com/austinuts-wholesale-inc-announces-voluntary-recall-of-pistachio-kernel-products</link>
		<comments>http://www.recallnewsletter.com/austinuts-wholesale-inc-announces-voluntary-recall-of-pistachio-kernel-products#comments</comments>
		<pubDate>Fri, 20 Aug 2010 20:24:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/austinuts-wholesale-inc-announces-voluntary-recall-of-pistachio-kernel-products</guid>
		<description><![CDATA[AustiNuts Wholesale, Inc. is issuing this voluntary recall of pistachio kernel products due to a recall that was issued by it&#8217;s supplier California Delights, Inc. California Delights, Inc issued a recall for two shipments of pistachio kernels received by AustiNuts Wholesale, Inc. in July 2010 due to the possibility of contamination with Salmonella. This is [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>AustiNuts Wholesale, Inc. is issuing this voluntary recall of pistachio kernel products due to a recall that was issued by it&#8217;s supplier California Delights, Inc.  California Delights, Inc issued a recall for two shipments of pistachio kernels received by AustiNuts Wholesale, Inc. in July 2010 due to the possibility of contamination with Salmonella.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223524.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Salmonella in Alfalfa Sprouts</title>
		<link>http://www.recallnewsletter.com/salmonella-in-alfalfa-sprouts</link>
		<comments>http://www.recallnewsletter.com/salmonella-in-alfalfa-sprouts#comments</comments>
		<pubDate>Fri, 20 Aug 2010 20:00:04 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/salmonella-in-alfalfa-sprouts</guid>
		<description><![CDATA[New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Snow White Food Products Inc., located in 621 Bergen Street in Brooklyn, New York, is recalling certain packages of &#8220;Alfalfa Sprouts&#8221; due to the presence of Salmonella. The recalled &#8220;Alfalfa Sprouts&#8221; is packaged in a 3.5 ounce plastic clamshell container which is uncoded. It [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Snow White Food Products Inc., located in 621 Bergen Street in Brooklyn, New York, is recalling certain packages of &#8220;Alfalfa Sprouts&#8221; due to the presence of Salmonella. The recalled &#8220;Alfalfa Sprouts&#8221; is packaged in a 3.5 ounce plastic clamshell container which is uncoded.  It has a UPC code of 0-46421-11236-6.  The product was distributed in New York State.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223487.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Urgent Nationwide Frozen Mamey Fruit Products Recall</title>
		<link>http://www.recallnewsletter.com/urgent-nationwide-frozen-mamey-fruit-products-recall</link>
		<comments>http://www.recallnewsletter.com/urgent-nationwide-frozen-mamey-fruit-products-recall#comments</comments>
		<pubDate>Fri, 20 Aug 2010 18:48:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/urgent-nationwide-frozen-mamey-fruit-products-recall</guid>
		<description><![CDATA[An investigation by the CDC and state partners showed an epidemiologic link between an ongoing outbreak of Salmonella Typhi and frozen mamey fruit products sold under the La Nuestra brand by Montalvan Sales Inc. Ontario, Calif, and under the Goya brand by Goya Foods Inc. Secaucus, New Jersey. This is a summary of a Press [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>An investigation by the CDC and state partners showed an epidemiologic link between an ongoing outbreak of Salmonella Typhi and frozen mamey fruit products sold under the La Nuestra brand by Montalvan Sales Inc. Ontario, Calif, and under the Goya brand by Goya Foods Inc. Secaucus, New Jersey.</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm223465.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<title>Hillandale Farms of Iowa Conducts Nationwide Voluntary Recall of Shell Eggs Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/hillandale-farms-of-iowa-conducts-nationwide-voluntary-recall-of-shell-eggs-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/hillandale-farms-of-iowa-conducts-nationwide-voluntary-recall-of-shell-eggs-because-of-possible-health-risk#comments</comments>
		<pubDate>Fri, 20 Aug 2010 18:24:04 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/hillandale-farms-of-iowa-conducts-nationwide-voluntary-recall-of-shell-eggs-because-of-possible-health-risk</guid>
		<description><![CDATA[Hillandale Farms of Iowa is voluntarily recalling shell eggs because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. This is a summary of a recall issued by the Food [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Hillandale Farms of Iowa is voluntarily recalling shell eggs because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223452.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>Stalevo(carbidopa/levodopa and entacapone): Ongoing Safety Review: Possible increased cardiovascular risk</title>
		<link>http://www.recallnewsletter.com/stalevocarbidopalevodopa-and-entacapone-ongoing-safety-review-possible-increased-cardiovascular-risk</link>
		<comments>http://www.recallnewsletter.com/stalevocarbidopalevodopa-and-entacapone-ongoing-safety-review-possible-increased-cardiovascular-risk#comments</comments>
		<pubDate>Fri, 20 Aug 2010 16:48:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[MedWatch]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/stalevocarbidopalevodopa-and-entacapone-ongoing-safety-review-possible-increased-cardiovascular-risk</guid>
		<description><![CDATA[FDA evaluating clinical trial data that suggest patients taking drug may be at an increased risk for cardiovascular events compared to those taking carbidopa/levodopa This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program. The link below will take you to the original notice. View Full [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>FDA evaluating clinical trial data that suggest patients taking drug may be at an increased risk for cardiovascular events<br />
compared to those taking carbidopa/levodopa</p>
<p>This is a summary of an alert issued by MedWatch: The FDA Safety Information and Adverse Event Reporting Program.  The link below will take you to the original notice.</p>
<p><a href="http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm223423.htm" target="_blank">View Full Details Of The Original MedWatch Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>Montalvan’s Sales, Inc. Recalls “La Nuestra” Brand Frozen Mamey Because of Potential Health Risk</title>
		<link>http://www.recallnewsletter.com/montalvan%e2%80%99s-sales-inc-recalls-%e2%80%9cla-nuestra%e2%80%9d-brand-frozen-mamey-because-of-potential-health-risk</link>
		<comments>http://www.recallnewsletter.com/montalvan%e2%80%99s-sales-inc-recalls-%e2%80%9cla-nuestra%e2%80%9d-brand-frozen-mamey-because-of-potential-health-risk#comments</comments>
		<pubDate>Fri, 20 Aug 2010 13:00:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/montalvan%e2%80%99s-sales-inc-recalls-%e2%80%9cla-nuestra%e2%80%9d-brand-frozen-mamey-because-of-potential-health-risk</guid>
		<description><![CDATA[As a precautionary measure, Montalvan’s Sales, Inc. of Ontario, CA has voluntarily recalled “La Nuestra” brand frozen mamey pulp due to a potential health risk from Salmonella Typhi. Typhoid fever is a life-threatening illness caused by the bacterium Salmonella Typhi. This is a summary of a recall issued by the Food and Drug Administration (FDA). [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>As a precautionary measure, Montalvan’s Sales, Inc. of Ontario, CA has voluntarily recalled “La Nuestra” brand frozen mamey pulp due to a potential health risk from Salmonella Typhi.  Typhoid fever is a life-threatening illness caused by the bacterium Salmonella Typhi.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223383.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Urgent Nationwide Egg Recall</title>
		<link>http://www.recallnewsletter.com/urgent-nationwide-egg-recall</link>
		<comments>http://www.recallnewsletter.com/urgent-nationwide-egg-recall#comments</comments>
		<pubDate>Fri, 20 Aug 2010 00:24:11 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/urgent-nationwide-egg-recall</guid>
		<description><![CDATA[• The current recall of eggs in their shells, or “shell eggs,” is part of an ongoing and intensive investigation by local, state, and federal officials into the cause of recent cases of Salmonella Enteritidis. This is a summary of a Press Release issued by the Food and Drug Administration (FDA). The link below will [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>•	The current recall of eggs in their shells, or “shell eggs,” is part of an ongoing and intensive investigation by local, state, and federal officials into the cause of recent cases of Salmonella Enteritidis.</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm223248.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<title>Consumer Advisory &#8211; Salmonella Contamination of Eggs in the United States</title>
		<link>http://www.recallnewsletter.com/consumer-advisory-salmonella-contamination-of-eggs-in-the-united-states</link>
		<comments>http://www.recallnewsletter.com/consumer-advisory-salmonella-contamination-of-eggs-in-the-united-states#comments</comments>
		<pubDate>Thu, 19 Aug 2010 23:24:07 +0000</pubDate>
		<dc:creator>CFIA</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Food Recalls Canada CFIA]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/consumer-advisory-salmonella-contamination-of-eggs-in-the-united-states</guid>
		<description><![CDATA[The Government of Canada is closely following an investigation by U.S. authorities into Salmonella contamination of eggs in the United States. This is a summary of a recall issued by the Canadian Food Inspection Agency. The link below will take you to the original recall press release containing complete information, including instructions about what to [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The Government of Canada is closely following an investigation by U.S. authorities into Salmonella contamination of eggs in the United States.</p>
<p>This is a summary of a recall issued by the Canadian Food Inspection Agency.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.inspection.gc.ca/english/corpaffr/newcom/2010/20100819e.shtml" target="_blank">View Full Details Of Original CFIA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<title>COUNTRY Eggs, Inc. Initiates Voluntary Recall of Large AA Loose 15 dozen Fresh Shell Eggs Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/country-eggs-inc-initiates-voluntary-recall-of-large-aa-loose-15-dozen-fresh-shell-eggs-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/country-eggs-inc-initiates-voluntary-recall-of-large-aa-loose-15-dozen-fresh-shell-eggs-because-of-possible-health-risk#comments</comments>
		<pubDate>Thu, 19 Aug 2010 20:24:10 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/country-eggs-inc-initiates-voluntary-recall-of-large-aa-loose-15-dozen-fresh-shell-eggs-because-of-possible-health-risk</guid>
		<description><![CDATA[The following statement was released by officials of Country Eggs, Inc. regarding the voluntary recall of shell eggs supplied from Wright County Egg of Galt, Iowa. Country Eggs, Inc. is voluntary recalling specific Julian dates of shell eggs produced by Wright County Egg of Galt, Iowa because they have the potential to be contaminated with [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The following statement was released by officials of Country Eggs, Inc. regarding the voluntary recall of shell eggs supplied from Wright County Egg of Galt, Iowa. Country Eggs, Inc. is voluntary recalling specific Julian dates of shell eggs produced by Wright County Egg of Galt, Iowa because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems&#8230;</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223328.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<title>Unauthorized ExtenZe Sexual Enhancement Supplements May Pose Health Risks</title>
		<link>http://www.recallnewsletter.com/unauthorized-extenze-sexual-enhancement-supplements-may-pose-health-risks</link>
		<comments>http://www.recallnewsletter.com/unauthorized-extenze-sexual-enhancement-supplements-may-pose-health-risks#comments</comments>
		<pubDate>Thu, 19 Aug 2010 19:48:09 +0000</pubDate>
		<dc:creator>Health Canada</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Health Canada Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/unauthorized-extenze-sexual-enhancement-supplements-may-pose-health-risks</guid>
		<description><![CDATA[Health Canada has seized the unauthorized sexual enhancement supplements &#8220;Male Enhancement ExtenZe&#8221; and &#8220;Women ExtenZe&#8221; (shown below) imported and sold by the Happy Paradise Adult Store in Burnaby, British Columbia. This is a summary of a recall issued by Health Canada. The link below will take you to the original recall press release containing complete [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Health Canada has seized the unauthorized sexual enhancement supplements &#8220;Male Enhancement ExtenZe&#8221; and &#8220;Women ExtenZe&#8221; (shown below) imported and sold by the Happy Paradise Adult Store in Burnaby, British Columbia.</p>
<p>This is a summary of a recall issued by Health Canada.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.hc-sc.gc.ca/ahc-asc/media/advisories-avis/_2010/2010_144-eng.php" target="_blank"><br />
View Full Details Of Original Health Canada Recall Notice Here<a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>U.S. Marshals seize food from rodent-infested Ga. warehouse</title>
		<link>http://www.recallnewsletter.com/u-s-marshals-seize-food-from-rodent-infested-ga-warehouse</link>
		<comments>http://www.recallnewsletter.com/u-s-marshals-seize-food-from-rodent-infested-ga-warehouse#comments</comments>
		<pubDate>Thu, 19 Aug 2010 18:48:10 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Alerts]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/u-s-marshals-seize-food-from-rodent-infested-ga-warehouse</guid>
		<description><![CDATA[U.S. Marshals, acting under a court order sought by the U.S. Food and Drug Administration, today seized packaged food products from a rodent-infested warehouse in Athens, Ga. A variety of products, including crackers, cookies and potato chips, were intended for sale to jails and prisons throughout the southeastern United States. This is a summary of [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>U.S. Marshals, acting under a court order sought by the U.S. Food and Drug Administration, today seized packaged food products from a rodent-infested warehouse in Athens, Ga. A variety of products, including crackers, cookies and potato chips, were intended for sale to jails and prisons throughout the southeastern United States.</p>
<p>This is a summary of a Press Release issued by the Food and Drug Administration (FDA).  The link below will take you to the original press release containing complete information, including instructions about what to do if you are affected.</p>
<p><a href="http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm223284.htm" target="_blank">View Full Details Of Original FDA Press Release Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>White Tiger Outdoor Folding Chairs Recalled Due to Fall Hazard</title>
		<link>http://www.recallnewsletter.com/white-tiger-outdoor-folding-chairs-recalled-due-to-fall-hazard</link>
		<comments>http://www.recallnewsletter.com/white-tiger-outdoor-folding-chairs-recalled-due-to-fall-hazard#comments</comments>
		<pubDate>Thu, 19 Aug 2010 14:24:05 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Household Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/white-tiger-outdoor-folding-chairs-recalled-due-to-fall-hazard</guid>
		<description><![CDATA[The wooden frame of the chairs can break, posing a fall hazard to consumers. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The wooden frame of the chairs can break, posing a fall hazard to consumers.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10322.html" target="_blank">View Full Details Of Original CSPC Recall Notice Here</a></p>
]]></content:encoded>
			<wfw:commentRss>http://www.recallnewsletter.com/white-tiger-outdoor-folding-chairs-recalled-due-to-fall-hazard/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
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		<title>Wright County Egg Expands Nationwide Voluntary Recall of Shell Eggs Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/wright-county-egg-expands-nationwide-voluntary-recall-of-shell-eggs-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/wright-county-egg-expands-nationwide-voluntary-recall-of-shell-eggs-because-of-possible-health-risk#comments</comments>
		<pubDate>Thu, 19 Aug 2010 12:24:10 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/wright-county-egg-expands-nationwide-voluntary-recall-of-shell-eggs-because-of-possible-health-risk</guid>
		<description><![CDATA[Wright County Egg of Galt, Iowa is expanding its voluntary recall (original recall date: August 13, 2010) of specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Wright County Egg of Galt, Iowa is expanding its voluntary recall (original recall date: August 13, 2010) of specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella.  Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.  Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain.  In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis or arthritis.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223139.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>NuCal Foods Conducts Recall of Shell Eggs Supplied from Wright County Egg Because of Possible Health Risk</title>
		<link>http://www.recallnewsletter.com/nucal-foods-conducts-recall-of-shell-eggs-supplied-from-wright-county-egg-because-of-possible-health-risk</link>
		<comments>http://www.recallnewsletter.com/nucal-foods-conducts-recall-of-shell-eggs-supplied-from-wright-county-egg-because-of-possible-health-risk#comments</comments>
		<pubDate>Thu, 19 Aug 2010 12:24:06 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/nucal-foods-conducts-recall-of-shell-eggs-supplied-from-wright-county-egg-because-of-possible-health-risk</guid>
		<description><![CDATA[NuCal Foods is voluntarily recalling specific Julian dates of shell eggs produced by Wright County Egg and packaged by NuCal Foods because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>NuCal Foods is voluntarily recalling specific Julian dates of shell eggs produced by Wright County Egg and packaged by NuCal Foods because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis or arthritis.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223140.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>J &amp; H Besta Expands Nationwide Recall of Slim- 30 Herb Supplement to Include Lot 6032101 Found to Contain an Undeclared Drug Ingredient</title>
		<link>http://www.recallnewsletter.com/j-h-besta-expands-nationwide-recall-of-slim-30-herb-supplement-to-include-lot-6032101-found-to-contain-an-undeclared-drug-ingredient</link>
		<comments>http://www.recallnewsletter.com/j-h-besta-expands-nationwide-recall-of-slim-30-herb-supplement-to-include-lot-6032101-found-to-contain-an-undeclared-drug-ingredient#comments</comments>
		<pubDate>Thu, 19 Aug 2010 11:57:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/j-h-besta-expands-nationwide-recall-of-slim-30-herb-supplement-to-include-lot-6032101-found-to-contain-an-undeclared-drug-ingredient</guid>
		<description><![CDATA[J &#38; H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Slim-30 Herb Supplement Lot 6032101 distributed by the company was found to contain undeclared Desmethyl Sibutramine, similar in structure to Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>J &amp; H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Slim-30 Herb Supplement Lot 6032101 distributed by the company was found to contain undeclared Desmethyl Sibutramine, similar in structure to Sibutramine.  Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss.   The FDA has not approved Slim-30 Herbal Supplement, therefore the safety and effectiveness of the product is unknown.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223141.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>MICRO BIRD ( 10V377000 )</title>
		<link>http://www.recallnewsletter.com/micro-bird-10v377000</link>
		<comments>http://www.recallnewsletter.com/micro-bird-10v377000#comments</comments>
		<pubDate>Thu, 19 Aug 2010 10:00:09 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/micro-bird-10v377000</guid>
		<description><![CDATA[Dated: AUG 12, 2010 CERTAIN GIRARDIN MODEL YEAR 2006 THROUGH 2010 AND MICRO BIRD BY GIRARDIN MODEL YEAR 2009 THROUGH 2010 G5 TRANSIT BUSES FAIL TO CONFORM TO THE REQUIREMENTS OF FEDERAL MOTOR VEHICLE SAFETY STANDARD NO. &#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 12, 2010 CERTAIN GIRARDIN MODEL YEAR 2006 THROUGH 2010 AND MICRO BIRD BY GIRARDIN MODEL YEAR 2009 THROUGH 2010 G5 TRANSIT BUSES FAIL TO CONFORM TO THE REQUIREMENTS OF FEDERAL MOTOR VEHICLE SAFETY STANDARD NO. &#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V377000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>GIRARDIN ( 10V377000 )</title>
		<link>http://www.recallnewsletter.com/girardin-10v377000</link>
		<comments>http://www.recallnewsletter.com/girardin-10v377000#comments</comments>
		<pubDate>Thu, 19 Aug 2010 10:00:08 +0000</pubDate>
		<dc:creator>NHTSA</dc:creator>
				<category><![CDATA[Auto Recalls-Vehicles]]></category>
		<category><![CDATA[Automobile & Related Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/girardin-10v377000</guid>
		<description><![CDATA[Dated: AUG 12, 2010 CERTAIN GIRARDIN MODEL YEAR 2006 THROUGH 2010 AND MICRO BIRD BY GIRARDIN MODEL YEAR 2009 THROUGH 2010 G5 TRANSIT BUSES FAIL TO CONFORM TO THE REQUIREMENTS OF FEDERAL MOTOR VEHICLE SAFETY STANDARD NO. &#8230; This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA). The [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Dated: AUG 12, 2010 CERTAIN GIRARDIN MODEL YEAR 2006 THROUGH 2010 AND MICRO BIRD BY GIRARDIN MODEL YEAR 2009 THROUGH 2010 G5 TRANSIT BUSES FAIL TO CONFORM TO THE REQUIREMENTS OF FEDERAL MOTOR VEHICLE SAFETY STANDARD NO. &#8230;</p>
<p>This is a summary of a recall issued by the National Highway Transportation Safety Administration (NHTSA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www-odi.nhtsa.dot.gov/recalls/results.cfm?rcl_id=10V377000&amp;searchtype=quicksearch&amp;summary=true&amp;refurl=rss" target="_blank">View Full Details Of Original NHTSA Recall Notice Here</a>.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>Lan Enterprises Recalls Zooper Tango Double Strollers Due to Collapse Hazard</title>
		<link>http://www.recallnewsletter.com/lan-enterprises-recalls-zooper-tango-double-strollers-due-to-collapse-hazard</link>
		<comments>http://www.recallnewsletter.com/lan-enterprises-recalls-zooper-tango-double-strollers-due-to-collapse-hazard#comments</comments>
		<pubDate>Thu, 19 Aug 2010 10:00:00 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Children's Toy Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/lan-enterprises-recalls-zooper-tango-double-strollers-due-to-collapse-hazard</guid>
		<description><![CDATA[The stroller&#8217;s frame latch above the front wheels can fail when the stroller hits an object, causing the stroller to unexpectedly collapse. This can result in minor scrapes, cuts and bruises. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The stroller&#8217;s frame latch above the front wheels can fail when the stroller hits an object, causing the stroller to unexpectedly collapse. This can result in minor scrapes, cuts and bruises.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10321.html" target="_blank"> View Full Details Of Original CPSC Recall Notice Here</a>, Including Pictures If Any.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Moonstruck Chocolate Co. Issues Nationwide Allergy Alert on Undeclared Peanut-Butter Filling in Their  4 Piece Cream Cone Chocolate Truffle Collection and 12 Piece Chocolate Malted (or Malt) Cream Cone Chocolate Truffles</title>
		<link>http://www.recallnewsletter.com/moonstruck-chocolate-co-issues-nationwide-allergy-alert-on-undeclared-peanut-butter-filling-in-their-4-piece-cream-cone-chocolate-truffle-collection-and-12-piece-chocolate-malted-or-malt-cream-con</link>
		<comments>http://www.recallnewsletter.com/moonstruck-chocolate-co-issues-nationwide-allergy-alert-on-undeclared-peanut-butter-filling-in-their-4-piece-cream-cone-chocolate-truffle-collection-and-12-piece-chocolate-malted-or-malt-cream-con#comments</comments>
		<pubDate>Thu, 19 Aug 2010 01:24:03 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/moonstruck-chocolate-co-issues-nationwide-allergy-alert-on-undeclared-peanut-butter-filling-in-their-4-piece-cream-cone-chocolate-truffle-collection-and-12-piece-chocolate-malted-or-malt-cream-con</guid>
		<description><![CDATA[Moonstruck Chocolate Co. of Portland, Oregon is voluntarily recalling their 4 piece Cream Cone Chocolate Truffle Collection and the 12 piece Chocolate Malted (or Malt) Cream Cone Chocolate Truffles, because they may contain undeclared peanut butter. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Moonstruck Chocolate Co. of Portland, Oregon is voluntarily recalling their 4 piece Cream Cone Chocolate Truffle Collection and the 12 piece Chocolate Malted (or Malt) Cream Cone Chocolate Truffles, because they may contain undeclared peanut butter.   People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume this product.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223131.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<item>
		<title>Glow Industries, Inc. Issues Nationwide Recall of Mr. Magic Male Enhancer from Don Wands Amended</title>
		<link>http://www.recallnewsletter.com/glow-industries-inc-issues-nationwide-recall-of-mr-magic-male-enhancer-from-don-wands-amended</link>
		<comments>http://www.recallnewsletter.com/glow-industries-inc-issues-nationwide-recall-of-mr-magic-male-enhancer-from-don-wands-amended#comments</comments>
		<pubDate>Wed, 18 Aug 2010 20:48:05 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/glow-industries-inc-issues-nationwide-recall-of-mr-magic-male-enhancer-from-don-wands-amended</guid>
		<description><![CDATA[Glow Industries, Inc., Perrysburg, OH, announced today that it is initiating a voluntary nationwide recall of the company&#8217;s product sold under the name of Mr. Magic Male Enhancer from Don Wands. Glow Industries, Inc. is conducting this voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found the [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Glow Industries, Inc., Perrysburg, OH, announced today that it is initiating a voluntary nationwide recall of the company&#8217;s product sold under the name of Mr. Magic Male Enhancer from Don Wands. Glow Industries, Inc. is conducting this voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found the Mr. Magic Male Enhancer from Don Wands capsules to contain Hydroxythiohomosildenafil and Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used in the treatment of male Erectile Dysfunction (ED), making Mr. Magic Male Enhancer an unapproved new drug. These active ingredients are not listed on the product label. Product manufactured containing lot numbers 9041401, 251209 and 8121904 are included in this recall&#8230;</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm223082.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Undeclared Sulfites in &quot;Golden Bridge&quot; Dried Dates</title>
		<link>http://www.recallnewsletter.com/undeclared-sulfites-in-golden-bridge-dried-dates</link>
		<comments>http://www.recallnewsletter.com/undeclared-sulfites-in-golden-bridge-dried-dates#comments</comments>
		<pubDate>Wed, 18 Aug 2010 20:00:07 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/undeclared-sulfites-in-golden-bridge-dried-dates</guid>
		<description><![CDATA[New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Sunny Lake Trading Inc, located at 651A Lexington Ave, Brooklyn, New York is recalling &#8220;Golden Bridge&#8221; dried dates due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Sunny Lake Trading Inc, located at 651A Lexington Ave, Brooklyn, New York is recalling &#8220;Golden Bridge&#8221; dried dates due to the presence of undeclared sulfites.  People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm222964.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Brigade Hickory Handle Sledge Hammers Recalled by White Cap Construction Supply Due to Risk of Injury</title>
		<link>http://www.recallnewsletter.com/brigade-hickory-handle-sledge-hammers-recalled-by-white-cap-construction-supply-due-to-risk-of-injury</link>
		<comments>http://www.recallnewsletter.com/brigade-hickory-handle-sledge-hammers-recalled-by-white-cap-construction-supply-due-to-risk-of-injury#comments</comments>
		<pubDate>Wed, 18 Aug 2010 19:24:02 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Household Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/brigade-hickory-handle-sledge-hammers-recalled-by-white-cap-construction-supply-due-to-risk-of-injury</guid>
		<description><![CDATA[The head of the sledge hammer can loosen and detach, posing a risk of impact injury to consumerss. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below will take you to the original recall press release containing complete information, including instructions about what to do if [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>The head of the sledge hammer can loosen and detach, posing a risk of impact injury to consumerss.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10320.html" target="_blank">View Full Details Of Original CSPC Recall Notice Here</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Electrical Wire Recalled by Cerro Wire due to Fire Hazard</title>
		<link>http://www.recallnewsletter.com/electrical-wire-recalled-by-cerro-wire-due-to-fire-hazard</link>
		<comments>http://www.recallnewsletter.com/electrical-wire-recalled-by-cerro-wire-due-to-fire-hazard#comments</comments>
		<pubDate>Wed, 18 Aug 2010 17:24:04 +0000</pubDate>
		<dc:creator>CPSC</dc:creator>
				<category><![CDATA[Household Recalls]]></category>
		<category><![CDATA[Toy & Product Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/electrical-wire-recalled-by-cerro-wire-due-to-fire-hazard</guid>
		<description><![CDATA[While the actual electrical wire has &#8220;14 gauge&#8221; printed on it, the packaging incorrectly labels the electrical wire as 12 gauge. If used as a 12 gauge wire, it can overload, posing a fire hazard to consumers. This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC). The link below [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>While the actual electrical wire has &#8220;14 gauge&#8221; printed on it, the packaging incorrectly labels the electrical wire as 12 gauge. If used as a 12 gauge wire, it can overload, posing a fire hazard to consumers.</p>
<p>This is a summary of a recall issued by the Consumer Product Safety Commission (CPSC).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.cpsc.gov/cpscpub/prerel/prhtml10/10319.html" target="_blank">View Full Details Of Original CSPC Recall Notice Here</a></p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Elie Baking Corp issues Allergy Alert on Undeclared Soy in Food City brand Low-Carb Tortilla White and Whole Wheat 10 count</title>
		<link>http://www.recallnewsletter.com/elie-baking-corp-issues-allergy-alert-on-undeclared-soy-in-food-city-brand-low-carb-tortilla-white-and-whole-wheat-10-count</link>
		<comments>http://www.recallnewsletter.com/elie-baking-corp-issues-allergy-alert-on-undeclared-soy-in-food-city-brand-low-carb-tortilla-white-and-whole-wheat-10-count#comments</comments>
		<pubDate>Wed, 18 Aug 2010 17:24:03 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Recalls]]></category>
		<category><![CDATA[Food Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/elie-baking-corp-issues-allergy-alert-on-undeclared-soy-in-food-city-brand-low-carb-tortilla-white-and-whole-wheat-10-count</guid>
		<description><![CDATA[Elie Baking Corp. dba Near East Baking Corporation, 204 N Montello St,, Brockton, Massachusetts is recalling the following: Food City brand, Low Carb Tortilla White, 13.5 oz, 10 count. UPC 0 87848 42002 0 Food City brand, Low Carb Tortilla Whole Wheat, 13.5 oz.10 count. UPC 0 87848 42003 0 MFG Date 07/21/10 &#38; MFG [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Elie Baking Corp. dba Near East Baking Corporation, 204 N Montello St,, Brockton, Massachusetts is recalling the following: Food City brand, Low Carb Tortilla White, 13.5 oz, 10 count. UPC 0 87848 42002 0<br />
Food City brand, Low Carb Tortilla Whole Wheat, 13.5 oz.10 count. UPC 0 87848 42003 0<br />
MFG Date 07/21/10 &amp; MFG Date 07/22/10 stamped on the top left of the bag.</p>
<p>This is a summary of a recall issued by the Food and Drug Administration (FDA).  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.fda.gov/Safety/Recalls/ucm222940.htm" target="_blank">View Full Details Of Original FDA Recall Notice Here.</a></p>
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		<title>Unauthorized Health Product: &quot;SeXXX DRIVE&quot; May Pose Serious Health Risks</title>
		<link>http://www.recallnewsletter.com/unauthorized-health-product-sexxx-drive-may-pose-serious-health-risks</link>
		<comments>http://www.recallnewsletter.com/unauthorized-health-product-sexxx-drive-may-pose-serious-health-risks#comments</comments>
		<pubDate>Wed, 18 Aug 2010 14:48:25 +0000</pubDate>
		<dc:creator>Health Canada</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Health Canada Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/unauthorized-health-product-sexxx-drive-may-pose-serious-health-risks</guid>
		<description><![CDATA[An unauthorized health product, &#8220;SeXXX DRIVE&#8221;, promoted as a herbal supplement to enhance male sexual performance, was tested by Health Canada and found to contain undeclared &#8220;hydroxyhomosildenafil&#8221;, a substance similar to the prescription medication sildenafil that may pose serious and potentially life-threatening health risks, particularly to people with heart problems. This is a summary of [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>An unauthorized health product, &#8220;SeXXX DRIVE&#8221;, promoted as a herbal supplement to enhance male sexual performance, was tested by Health Canada and found to contain undeclared &#8220;hydroxyhomosildenafil&#8221;, a substance similar to the prescription medication sildenafil that may pose serious and potentially life-threatening health risks, particularly to people with heart problems.</p>
<p>This is a summary of a recall issued by Health Canada.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.hc-sc.gc.ca/ahc-asc/media/advisories-avis/_2010/2010_143-eng.php" target="_blank"><br />
View Full Details Of Original Health Canada Recall Notice Here<a>.</p>
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		<title>Health Canada Statement on Radiofrequency Energy and Wi-Fi Equipment</title>
		<link>http://www.recallnewsletter.com/health-canada-statement-on-radiofrequency-energy-and-wi-fi-equipment</link>
		<comments>http://www.recallnewsletter.com/health-canada-statement-on-radiofrequency-energy-and-wi-fi-equipment#comments</comments>
		<pubDate>Wed, 18 Aug 2010 13:20:00 +0000</pubDate>
		<dc:creator>Health Canada</dc:creator>
				<category><![CDATA[Canadian Recalls]]></category>
		<category><![CDATA[Health Canada Recalls]]></category>

		<guid isPermaLink="false">http://www.recallnewsletter.com/health-canada-statement-on-radiofrequency-energy-and-wi-fi-equipment</guid>
		<description><![CDATA[Based on scientific evidence, Health Canada has determined that exposure to low-level radiofrequency energy, such as that from Wi-Fi systems, is not dangerous to the public. This is a summary of a recall issued by Health Canada. The link below will take you to the original recall press release containing complete information, including instructions about [...]]]></description>
			<content:encoded><![CDATA[<p></p><p>Based on scientific evidence, Health Canada has determined that exposure to low-level radiofrequency energy, such as that from Wi-Fi systems, is not dangerous to the public.</p>
<p>This is a summary of a recall issued by Health Canada.  The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.</p>
<p><a href="http://www.hc-sc.gc.ca/ahc-asc/media/ftr-ati/_2010/2010_142-eng.php" target="_blank"><br />
View Full Details Of Original Health Canada Recall Notice Here<a>.</p>
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