For example, 200,000 infusion pumps were involved in a Class I recall by Baxter International in Jan. 2009, identifying software and battery failures. The recall allowed for continued use of affected pumps at hospitals and other facilities that filled out the necessary paperwork, but this extension will end in July 2012.
The FDA has logged more than 56,000 infusion pump problems linked to 710 patient deaths.
Read the DotMed report on the FDA infusion pump recall.
Related Articles on Recalls of Infusion Pumps:
Medtronic Issues Warning for SynchroMed II Implantable Painkiller Pumps
FDA Orders Recall of Baxter’s Colleague Volumetric Infusion Pumps
FDA Launches New Initiative to Address Infusion Pump Safety Issues
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