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FDA Makes Class I Recall for Hospira, Inc. (HSP)'s Symbiq's Infusion Pumps


7/16/2010 7:39:55 AM

MedPage Today -- WASHINGTON -- The FDA initiated a class I recall -- its strictest -- of two infusion pumps released by a single company, due to a device error which may fail to recognize in-line air in infusions.

Read at MedPageToday

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