Reported Dec 28, 2016 · Terminated

AbbVie PEG Kit 20 FR

AbbVie Inc.

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: AbbVie Inc. · 1 N Waukegan Rd · North Chicago, IL · 60064-1802

Is this the product you have?

  • AbbVie PEG Kit 20 FR
Lot codes and dates
  • AbbVie PEG Kit 20 Fr Product
  • Code 62912-01-16 with lot numbers
    • 32025245
    • 32265215
    • 32335206
    • 32335336
Amount recalled
541 units

Where it was sold

Why it was recalled

AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors.

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 Jul 9, 2019 · Data as of Sep 19, 5:20 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.