Reported Feb 6, 2013 · Terminated

Infinity Enteralite Ambulatory Feeding Pumps, List number: INFKIT2 - Addendum to Operator's Manual Product usage:…

MOOG Medical Devices Group

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: MOOG Medical Devices Group · 4314 Zevex Park Ln · Salt Lake City, UT · 84123-7881

Is this the product you have?

  • Infinity Enteralite Ambulatory Feeding Pumps
  • List numberINFKIT2 - Addendum
  • to Operator's Manual Product usageprovide a means for the volumetric delivery of fluids used in Enteral applications
Lot codes and dates
  • List numberINFKIT2
  • Lot/Serial numbers

    2,960 of 2,960 codes

    • 105068015
    • 105068002
    • 105068014
    • 105068013
    • 105068012
    • 105068011
    • 105068009
    • 105068008
    • 105068007
    • 105066024
    • 105066021
    • 105068003
    • 105068005
    • 105068006
    • 105066004
    • 105068027
    • 105068028
    • 105068026
    • 105068019
    • 105068020
    • 105068031
    • 105068037
    • 105068023
    • 105068025
    • 105068034
    • 105068018
    • 105068017
    • 105068016
    • 105068033
    • 105068032
    • 105068030
    • 105068029
    • 105068036
    • 105068035
    • 105068022
    • 105068038
    • 105069005
    • 105069004
    • 105069003
    • 105069002
    • 105069001
    • 105069008
    • 105069007
    • 105069006
    • 105068039
    • 105068040
    • 105068041
    • 105069009
    • 105069014
    • 105069013
    • 105069012
    • 105069010
    • 105069011
    • 105070009
    • 105070008
    • 105070001
    • 105070010
    • 105070011
    • 105070003
    • 105070004
Amount recalled
92,488 units

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 10, 2014 · Data as of Sep 19, 5:26 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.