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WalkMed Infusion, LLC recalls Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for
Recalled March 12, 2014 · FDA recall Z-1122-2014 · WalkMed Infusion
Hazard
WalkMed Infusion is initiaing a recall on their Triton FP Infusion Pump, Part Number 400000 due to the label on the right side of the pump containing an incorrect instruction. · FDA Class II
Units
797
Sold at
US Distribution including the states of IL, MA, KS, and, NJ.
Description
WalkMed Infusion is initiaing a recall on their Triton FP Infusion Pump, Part Number 400000 due to the label on the right side of the pump containing an incorrect instruction.
Product
Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for delivering infusions of medications, as well as providing TPN (Total Parenteral Nutrition) and PCA (Patient Control Analgesia). It is intended for use in hospitals, ambulatory & nursing home (extended care) settings, and home care environments.
Manufacturer(s)
WalkMed Infusion, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →