Symbiq One-Channel Infuser and Symbiq Two-Channel Infuser - Class I Recall
MedSun: Newsletter #51, August 2010

FDA Medical Device Recalls

There is potential for the device to fail to detect air in line at the end of an infusion. Hospira mailed clinical bulletins to affected customers on April 9, 2010, and an updated clinical bulletin on June 11, 2010. In the June 11, 2010 letter, Hospira states the user does not have to remove or stop using the Symbiq infusion pump. Hospira also provided recommended mitigation actions for users.

Additional Information:

FDA Medical Device Recalls. Symbiq One-Channel Infuser and Symbiq Two-Channel Infuser. July 15, 2010.
http://www.fda.gov/MedicalDevices/Safety/RecallsCorrectionsRemovals/ListofRecalls/ucm219194.htm


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