Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0764-2013 — 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.

U.S. FDA — Device Enforcement · United States · 2012-10-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0764-2013
Date of alert: 2012-10-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: MOOG Medical Devices Group
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 105068015

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Recall Z-0764-2013 — 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.

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