Smiths Medical Medfusion Model 4000 Syringe Infusion Pump: Class I Recall – System Errors May Cause Device Shutdown

by FDA on August 3, 2012

in MedWatch

Delay or interruption of infusion therapy could result in serious injury and/or 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.

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