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MOOG Medical Devices Group recalls Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: pr
Recalled February 6, 2013 · FDA recall Z-0764-2013 · MOOG Medical Devices Group
Hazard
The firm is adding an addendum to the operator's manual for Infinity Enteralite Ambulatory Feeding Pumps pertaining to the Infinite Dose mode and the inability of the Pump to detect air in line. · FDA Class II
Units
92,488 units
Sold at
Worldwide Distribution and US Nationwide in the countries of (Germany, Sweeden, Croatia, Lithuania, and Dubai).
Description
The firm is adding an addendum to the operator's manual for Infinity Enteralite Ambulatory Feeding Pumps pertaining to the Infinite Dose mode and the inability of the Pump to detect air in line.
Product
Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage: provide a means for the volumetric delivery of fluids used in Enteral applications.
Manufacturer(s)
MOOG Medical Devices Group
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →