If a drug product marketed as sterile has microbial contamination, patient is at risk of serious infection.

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.

The U.S. Food and Drug Administration is alerting health care providers of concerns about a lack of sterility assurance of all sterile drug products made and distributed by NuVision Pharmacy of Dallas, Texas. The FDA recommends that these products should not be administered to patients.

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.

View Full Details Of Original FDA Press Release Here.

Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 18, 2013 Forest River is recalling certain model year 2013-2014 Forest River models Blue Ridge, Cardinal, Cherokee, Columbus, EVO, Georgetown, Flagstaff, Forester, Lexington, Puma, Rockwood, Sabre, Salem, Sand…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 09, 2013 Gulf Stream Coach is recalling certain model year 2001 Ultra, Conquest, Independence, Ultra Supreme, Yellowstone, and Cavalier motorhomes with floorplans 6316 or 8325. The motorhomes were manufacture…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 13, 2013 Maserati North America, Inc. (Maserati) is recalling certain model year 2005-2008 Quattroporte, 2008 Granturismo, and 2008 Alfa Romeo 8C vehicles. The rear tie rod assemblies may have insufficient an…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 13, 2013 Maserati North America, Inc. (Maserati) is recalling certain model year 2005-2008 Quattroporte, 2008 Granturismo, and 2008 Alfa Romeo 8C vehicles. The rear tie rod assemblies may have insufficient an…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 10, 2013 Mack Trucks, Inc. is recalling certain model year 2013-2014 CHU, CXU, GU, MRU, and LEU trucks manufactured July 16, 2012, through march 18, 2013 and equipped with drum brakes. The clevis pin for the …

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 01, 2013 New Heights LLC (New Heights) is recalling certain Equipter RB4000 dump trailers manufactured December 8, 2011, through December 21, 2011. These vehicles are equipped with Carlisle hydraulic brake ac…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 08, 2013 Magic Tilt Trailers is recalling certain boat trailers manufactured October 17, 2011, through January 24, 2012. These trailers are equipped with brake actuators manufactured by Carlisle. On some of t…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 06, 2013 Elgin Sweeper Company Inc. (Elgin) is recalling certain model year 2006-2012 Crosswind J Alternative Fuel street sweepers, serial numbers J3285, J3260D, J3261D, J3300D, J3367, J3368D, J3370D, J3385D, …

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.

View Full Details Of Original NHTSA Recall Notice Here.

Patients are at increased risk of infection in the event a sterile product is compromised.

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.

The U.S. Department of Justice, on behalf of the U.S. Food and Drug Administration (FDA), is seeking a preliminary injunction in the U.S. District Court for the Eastern District of New York against New York City Fish, Inc., and several key employees for manufacturing and distributing ready-to-eat fish products under insanitary conditions causing them to become adulterated.

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.

View Full Details Of Original FDA Press Release Here.

Pentec Health, Inc. has decided to initiate a limited, voluntary recall of in-date nutritional prescriptions for renal patients due to lack of sterility assurance associated with one of its laminar flow hoods used in compounding.

The recall covers renal therapies that were compounded in this hood on or before May 2, 2013.

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.

View Full Details Of Original FDA Recall Notice Here.

Tropical Valley Foods Inc. of Plattsburgh, NY, is recalling next by Nature DARK CHOCOLATE BANANAS, 3 oz. bags, due to undeclared milk and walnuts. People who have an allergy to milk and/or walnuts run the risk of serious or life-threatening allergic reaction if they consume this product.

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.

View Full Details Of Original FDA Recall Notice Here.

Rural King Distributing of Mattoon, IL is recalling 205 tons of Deer Corn, because it has the potential to be contaminated with aflatoxin. Aflatoxin is a naturally occurring mold by-product.

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.

View Full Details Of Original FDA Recall Notice Here.

Dated: MAY 07, 2013 Temsa Global is recalling certain model year 2011-2013 model year TS35C coach buses manufactured from November 2010, through February 2013. Due to a production process error, the fuel tank may develo…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 02, 2013 Kovatch Mobile Equipment Corp. (Kovatch) is recalling certain model year 2009-2013 Predator, Predator SS, Panther; 2010-2011 ARFF; and model year 2010-2013 Panther II emergency vehicles. The grease f…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 06, 2013 Heartland Recreational Vehicles (Heartland) is recalling certain model year 2013-2014 Sundance travel trailers, model 322RES, manufactured September 13, 2012, through April 30, 2013. The axles are mo…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 08, 2013 Autocar, LLC is recalling certain model year 2005-2013 ACX, WX, and WXLL trucks built November 16, 2004, through September 10, 2012. On the affected vehicles, the air brake systems were built without…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 08, 2013 Autocar, LLC is recalling certain model year 2012-2013 ACX trucks built May 1, 2012, through November 15, 2012. Due to an insufficient weld, the windshield wiper arms of the vehicles may not be held …

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.

View Full Details Of Original NHTSA Recall Notice Here.

The recalling firm is True World Foods Inc. of Canada. This product has been distributed in British Columbia.

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.

View Full Details Of Original CFIA Recall Notice Here.

Various retailers. This product has been distributed in New Brunswick, Ontario, and Quebec.

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.

View Full Details Of Original CFIA Recall Notice Here.

May 10, 2013 – Symbios Medical Products initiated a voluntary recall of all GoPump Rapid Recovery System kits and GOBlock Kits manufactured with flow control components assembled prior to July 2012. These products have been found to potentially cause excessively high flow rates, which presents a risk of patient toxicity and serious injury (e.g., seizure, dysrhythmia, death) due to the rapid influx of medication particularly in patients with low body mass or advanced age.

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.

View Full Details Of Original FDA Recall Notice Here.

Bean bag chairs without a permanent zipper closure allow young children to unzip, ingest or inhale the small beads inside the bean bag chair.

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.

View Full Details Of Original CSPC Recall Notice Here

When cooked too long, the popcorn can overheat in the plastic popcorn maker and ignite.

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.

View Full Details Of Original CSPC Recall Notice Here

The hoodies were sold with drawstrings, which pose a hazard to young children.

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.

View Full Details Of Original CPSC Recall Notice Here, Including Pictures If Any.

Dated: APR 26, 2013 Fleetwood RV, Inc. is recalling certain model year 2013 Jamboree Sport Diesel, Providence, Tioga DSL and Tioga Ranger DSL; 2014 Excursion, Expedition, Jamboree Sport, Montara Commercial, Searcher Comm…

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.

View Full Details Of Original NHTSA Recall Notice Here.

The U.S. Food and Drug Administration today approved a new use for Simponi (golimumab) injection to treat adults with moderate to severe ulcerative colitis.

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.

View Full Details Of Original FDA Press Release Here.

The portable electric space heater’s design can fail to prevent ignition of nearby combustible materials.

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.

View Full Details Of Original CSPC Recall Notice Here

The U.S. Food and Drug Administration today approved Xofigo (radium Ra 223 dichloride) to treat men with symptomatic late-stage (metastatic) castration-resistant prostate cancer that has spread to bones but not to other organs. It is intended for men whose cancer has spread after receiving medical or surgical therapy to lower testosterone.

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.

View Full Details Of Original FDA Press Release Here.

Dated: MAY 13, 2013 Subaru is recalling certain model year 2013 Outback and Legacy vehicles manufactured from February 15, 2012, through June 15, 2012. In the affected vehicles, the inner and outer shafts of the steerin…

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.

View Full Details Of Original NHTSA Recall Notice Here.

The recalling firm is Chocolat Jean-Talon Chocolate Inc.. These products have been distributed in Alberta, Manitoba, New Brunswick, Newfoundland, Nova Scotia, Ontario, and Quebec and possibly nationally.

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.

View Full Details Of Original CFIA Recall Notice Here.

On May 10, the U.S. Food and Drug Administration approved Nymalize, a new nimodipine oral solution, to treat patients experiencing symptoms resulting from ruptured blood vessels in the brain (subarachnoid hemorrhage). Nimodipine previously was available only as a liquid-filled gel capsule.

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.

View Full Details Of Original FDA Press Release Here.

Dated: MAY 02, 2013 Tiffin Motorhomes, Inc. (Tiffin) is recalling certain model year 2013 Breeze and Allegro motorhomes. If the awning installation sequence was not completely followed, the awning motor may unknowingly …

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 07, 2013 Spartan Motors Chassis (Spartan) is recalling certain model year 2006-2011 K2, and K3 and 2006-2010 MM motorhome chassis manufactured July 20, 2005, through December 17, 2010. The steering gear mount…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 07, 2013 Heartland Recreational Vehicles is recalling certain model year 2013-2014 Big Country, Bighorn, Elk Ridge, Elk Ridge Express, Landmark, Prowler, Sundance, Sundance XLT, and Silverado fith wheel and tr…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 06, 2013 Lion Bus, Inc. is recalling one model year 2014 360 bus manufactured in December 2012. Due to insufficient distance between the air compressor discharge line and the hydraulic brake line, the lines m…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 23, 2013 Setra Luxury Coaches (Setra) is recalling certain model year 2011 through 2013 Setra S417 TC motorcoaches manufactured between May 2009 and March 2013 and model year 2012 and 2013 S407 motorcoaches ma…

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.

View Full Details Of Original NHTSA Recall Notice Here.

The U.S. Food and Drug Administration has released a new tool to help bolster the food industry’s defense measures against an act of intentional food contamination. The Food Defense Plan Builder is a comprehensive, easy-to-use software program designed to help owners and operators of food facilities—ranging from primary production and manufacturing to retail and transportation—develop customized plans to minimize the risk of intentional contamination at their individual food facilities.

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.

View Full Details Of Original FDA Press Release Here.

Advisories, public warnings and foreign product recalls are no longer part of the Media Room RSS Feed. Notices of advisories, public warnings and foreign product recalls are now available as a new separate RSS Feed titled “Healthy Canadians – Recalls and Safety Alerts – Health Canada – Media Room”. Please subscribe to this new RSS Feed to continue to receive notices about advisories, public warnings and foreign product recalls.

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.

View Full Details Of Original Health Canada Recall Notice Here.

Dated: MAY 07, 2013 Chrysler Group LLC (Chrysler) is recalling certain model year 2005-2010 Jeep Grand Cherokee vehicles manufactured February 11, 2004, through March 9, 2010; and 2006-2010 Jeep Commander vehicles manufa…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 07, 2013 Chrysler Group LLC (Chrysler) is recalling certain model year 2008-2012 Jeep Wrangler right-hand drive vehicles manufactured February 1, 2007, through October 10, 2011. The affected vehicles have air…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 30, 2013 Triumph Motorcycles America, Ltd. is recalling certain model year 2012-2013 Explorer and Explorer XC motorcycles. The Gross Vehicle Weight Rating data on the certification Label is incorrect. Thus, t…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 06, 2013 Dutchmen Manufacturing is recalling certain model year 2013 Breckenridge recreational vehicles manufactured February 13, 2013, through April 9, 2013. If the awning installation sequence was not compl…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 01, 2013 Volvo Bus Corporation is recalling certain model year 2009-2013 9700 coaches manufactured from August 28, 2008, through April 19, 2013. Certain conditions may cause the affected coaches to go into a …

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.

View Full Details Of Original NHTSA Recall Notice Here.

The recalling firm is Mitchell Agencies/Concord National. This product has been distributed in Newfoundland and Labrador and Quebec.

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.

View Full Details Of Original CFIA Recall Notice Here.

May 10, 2013 – Weston, Florida: Apotex Corp. announced today that it is conducting, on behalf of the manufacturer Hospira, Inc., a voluntary nationwide recall of 21 lots of Piperacillin and Tazobactam for Injection, USP 40.5 grams, NDC number 60505-0773-00 to the hospital / healthcare provider /user level. The impacted lots of Piperacillin and Tazobactam for Injection, USP 40.5 grams may show precipitation / crystallization in IV bag or IV line after reconstitution.

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.

View Full Details Of Original FDA Recall Notice Here.

The recalling firm is Canada Safeway Ltd.. This product has been distributed in Alberta, British Columbia, Manitoba, Ontario, and Saskatchewan.

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.

View Full Details Of Original CFIA Recall Notice Here.

Queen Creek, AZ, BeaMonstar Products is voluntarily recalling all of SexVoltz brand SKU’s 626570609490, 827912089028, 626570617877, 626570615316, 626570615316 Velextra brand SKU’s 626570613855, 626570619055, 626570617860, 626570617563 Amerect SKU’s 626570619031, 626570619628 capsules to the consumer level. Laboratory analysis conducted by the FDA on SexVoltz and Velextra has determined these products contain undeclared tadalafil. Amerect is voluntarily recalled because it has the potential to contain undeclared tadalafil. Tadalafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the products unapproved new drugs.

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.

View Full Details Of Original FDA Recall Notice Here.

Hannaford Supermarkets is recalling two products sold in the bakery section because they may contain nuts that are not listed on the product packaging label. Individuals who have an allergy or severe sensitivity to any nuts may run the risk of serious or life-threatening allergic reaction should they consume these items.

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.

View Full Details Of Original FDA Recall Notice Here.

Smart & Final of Los Angeles, Calif., which previously announced a recall of certain production dates of 2.5 lb – La Romanella Tri-Color Cheese Tortellini, is expanding its recall to include additional production dates due to undeclared wheat, eggs and milk. People who have an allergy or severe sensitivity to wheat, eggs and/or milk run the risk of serious or life-threatening allergic reaction if they consume these products.

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.

View Full Details Of Original FDA Recall Notice Here.

Touch Point-brand portable electric baseboard convection heaters with a model number of BBC-1500 can overheat.

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.

View Full Details Of Original CSPC Recall Notice Here

The Compounding Shop, LLC is conducting a voluntary recall of all lots of sterile products compounded by the pharmacy that are not expired. The recall is being initiated due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.

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.

View Full Details Of Original FDA Recall Notice Here.

The U.S. Food and Drug Administration is warning consumers not to consume any juice products or other beverages from Juices Incorporated (aka Juices International and Juices Enterprises) of Brooklyn, N.Y. The company’s carrot and beet juice products have the potential to be contaminated with Clostridium botulinum, a bacterium which can cause botulism, a serious and potentially fatal foodborne illness. Consumers are warned not to consume these products even if they do not look or smell spoiled.

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.

View Full Details Of Original FDA Press Release Here.

The U.S. Food and Drug Administration today approved Breo Ellipta (fluticasone furoate and vilanterol inhalation powder) for the long-term, once-daily, maintenance treatment of airflow obstruction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and/or emphysema. It is also approved to reduce exacerbations of COPD in patients with a history of exacerbations.

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.

View Full Details Of Original FDA Press Release Here.

Krinos Foods, LLC. of Long Island City, New York is voluntarily recalling its TAHINI sesame paste, 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. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

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.

View Full Details Of Original FDA Recall Notice Here.

Dairy Fresh is voluntarily recalling a specific batch of IGA Brand “Vanilla & Chocolate” Ice Cream (1.75 quart, 1.66L) with the plant code “3783” and a SELL BY date of 08-13-13 because it incorrectly contains Heavenly Hash ice cream, which contains almonds, coconut, and soy, which are allergens not declared on the carton. People who have an allergy or severe sensitivity to almonds, coconut, or soy run the risk of serious or life-threatening allergic reaction if they consume this product.

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.

View Full Details Of Original FDA Recall Notice Here.

May 9, 2013 – CAMBRIDGE, MA. – Whole Foods Market is recalling bulk curried chicken salad and bulk vegan curried chick’n salad because in some stores these items may have been sold with reversed labels causing undeclared soy and egg allergens. Due to the label mix-up, allergens were undeclared; the vegan chick’n salad contains soy, and the curried chicken salad contains egg.

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.

View Full Details Of Original FDA Recall Notice Here.

Today, Pure Herbs Ltd., Sterling Heights, MI is voluntarily recalling the 4oz and 1oz bottles of Protein Extract because they contain undeclared allergens – milk and soy. This labeling error was discovered during a routine Food and Drug Administration (FDA) inspection when a review of the ingredients found that milk and soy allergen ingredients were not listed on our main label.

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.

View Full Details Of Original FDA Recall Notice Here.

Bimeda Inc., on behalf of the manufacturer, Bimeda-MTC Animal Health Inc. is voluntarily recalling one lot of Calcium Gluconate, one lot of Dextrose 50%, and one lot of Hypertonic Saline, all of which are in the form of injectable fluids, to the user level. These injectable fluids are being recalled as a precautionary measure; because of departures from customary sterility procedures, sterility cannot be entirely assured.

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.

View Full Details Of Original FDA Recall Notice Here.

Risk of serious or life-threatening allergic reaction.

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.

The idler pulley on Z Master mowers can rub against the fuel tank. This is the second recall of these lawn mowers.

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.

View Full Details Of Original CSPC Recall Notice Here.

The brand name Optimus and two temperature knobs appear on the portable electric heaters.

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.

View Full Details Of Original CSPC Recall Notice Here

Dated: APR 30, 2013 Newmar Corporation is recalling certain model year 2012-2013 Canyon Star motorhomes manufactured August 4, 2011, through February 19, 2013, for failing to conform to the requirements of Federal Motor …

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 30, 2013 Newmar Corporation is recalling certain model year 2013 Bay Star Sport, Ventana and Ventana LE and model year 2013-2014 Bay Star, Canyon Star and Dutch Star motorhomes. If the awning installation seq…

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.

View Full Details Of Original NHTSA Recall Notice Here.

The recalling firm is Rococo Fine Foods Inc.. These products have been distributed nationally.

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.

View Full Details Of Original CFIA Recall Notice Here.

The recalling firm is Hapi Foods Group Inc.. This product has been distributed nationally.

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.

View Full Details Of Original CFIA Recall Notice Here.

These products should not be administered to patients. If a drug product marketed as sterile has microbial contamination, it potentially places patients at risk of serious infection.

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.

Nutraceutical company XYMOGEN in Orlando, Fla., is recalling artriphen, a product recommended for the support of healthy joint function, because it contains traces of the undeclared allergens soy and milk.

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.

View Full Details Of Original FDA Recall Notice Here.

The Honourable Leona Aglukkaq, Minister of Health, today announced that Canada’s Food and Drug Regulations have been amended to extend the requirements for Good Manufacturing Practices (GMP) to active ingredients (AI) used in pharmaceutical drugs. These amendments will come into force in the fall of this year.

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.

View Full Details Of Original Health Canada Recall Notice Here.

Surly Pugsley bike forks can bend above the disc brake mount.

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.

View Full Details Of Original CSPC Recall Notice Here.

Surly Pugsley bike forks can bend above the disc brake mount.

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.

View Full Details Of Original CSPC Recall Notice Here.

Undeclared tadalafil may interact with nitrates found in some prescription drugs such as nitroglycerin and may 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 notice.

View Full Details Of The Original MedWatch Notice Here.

Queen Creek, AZ, BeaMonstar Products is voluntarily recalling all of SexVoltz brand SKU’s 626570609490, 827912089028, 626570617877, 626570615316, Velextra brand SKU’s 626570619475, 626570619475, 626570619475, 626570619475 , Amerect SKU’s 626570619031, 626570619598 capsules to the retail level. Laboratory analysis conducted by the FDA on SexVoltz and Velextra has determined these products contain undeclared tadalafil. Amerect is voluntarily recalled because it has the potential to contain undeclared tadalafil. Tadalafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the products unapproved new drugs.

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.

View Full Details Of Original FDA Recall Notice Here.

Testing revealed the product contains tadalafil, which may interact with nitrates found in some prescription drugs, such as nitroglycerin, and may 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 notice.

View Full Details Of The Original MedWatch Notice Here.

Testing revealed the product contains an analogue of sildenafil, which may interact with nitrates found in prescription drugs such as nitroglycerin, 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 notice.

View Full Details Of The Original MedWatch Notice Here.

May result in unexpected ventilator shut downs, which can result in serious adverse health consequences, including death.

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.

The recalling firm is Ah Fong Food Products Ltd.. These products have been distributed in Ontario.

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.

View Full Details Of Original CFIA Recall Notice Here.

Use of lead cap may cause damage to lead.

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.

2013 Chang Kwung announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplements sold under the brand name Lightning Rod 500 mg per capsule packaged in 3-count, UPC 6 89076 20257 2 and 12-count bottles, UPC 6 89076 20297 8.
Chang Kwung is conducting a voluntary recall after being notified by the US FDA that analytical testing found the Lightning Rod Capsules to contain an analogue of Sildenafil.

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.

View Full Details Of Original FDA Recall Notice Here.

Use of these non-sterile products could increase the risk of infection in surgical 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 Original MedWatch Notice Here.

Plastic packaging may become lodged in the filter potentially causing an obstruction in airflow, which may result in low blood oxygen (hypoxia), suffocation and death.

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.

Dated: MAY 03, 2013 BMW is recalling certain model year 2002-2003 325i, 325xi, 330i, 330xi sedans; 325Ci and 330Ci coupes and convertibles; 325iT and 325xiT Sports Wagons; and M3 coupes and convertibles to address a safe…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 03, 2013 General Motors (GM) is recalling certain model year 2012 and 2013 Buick LaCrosse and Regal, and model year 2013 Chevrolet Malibu Eco vehicles equipped with eAssist. These vehicles may have a conditio…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: MAY 03, 2013 General Motors (GM) is recalling certain model year 2012 and 2013 Buick LaCrosse and Regal, and model year 2013 Chevrolet Malibu Eco vehicles equipped with eAssist. These vehicles may have a conditio…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 29, 2013 Westmor Industries, LLC. (Westmor) is recalling certain model year 2003-2013 trailers equipped with Fisher-branded H732 and H832 pressure relief valves, manufactured by Emerson Process Management Regu…

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.

View Full Details Of Original NHTSA Recall Notice Here.

Dated: APR 30, 2013 Kumho Tire U.S.A., Inc. (Kumho) is recalling certain Kumho Solus KH25 passenger car tires, size 225/45R17, produced in the weeks of 3411 through 2512 (August 21, 2011 through June 23, 2012). The aff…

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.

View Full Details Of Original NHTSA Recall Notice Here.

The recalling firm is Hevy D’s Old Fashioned Kettle Korn. This product has been distributed in AB, BC, MB, ON and SK

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.

View Full Details Of Original CFIA Recall Notice Here.

Cargill’s animal nutrition business today announced a voluntary recall of Showmaster® S-Series Show Lamb Feed (BW) because it contained incorrect sodium molybdate levels. To date, there are 170, 50-pound bags of feed still out in the market.

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.

View Full Details Of Original FDA Recall Notice Here.

Today, the U.S. Food and Drug Administration issued a proposed order that, if finalized, would reclassify sunlamp products and require labeling to include a recommendation designed to warn young people not to use these devices.

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.

View Full Details Of Original FDA Press Release Here.

Based on a recent study, there is evidence that these medications can cause decreased IQ scores in children whose mothers took them while pregnant.

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.

The U.S. Food and Drug Administration is alerting health care providers and patients that medications including and related to valproate sodium can cause decreased IQ scores in children whose mothers took the medication during pregnancy. Therefore, these drugs are being contraindicated for (should never be used by) pregnant women for the prevention of migraine headaches. Valproate products include valproate sodium (Depacon), divalproex sodium (Depakote, Depakote CP, and Depakote ER), valproic acid (Depakene and Stavzor), and their generics.

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.

View Full Details Of Original FDA Press Release Here.

Today, the Honourable Leona Aglukkaq, Minister of Health, acknowledged three exceptional nurses for their dedication, initiative and high standard of excellence in service to First Nations and Inuit communities.

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.

View Full Details Of Original Health Canada Recall Notice Here.