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.
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.
