Reported Apr 14, 2021 · Completed

Enteral Infusion Pump

Cardinal Health 200, LLC

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: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337

Is this the product you have?

  • Enteral Infusion Pump
Lot codes and dates
  • Catalog Number
    • 612054
    • 613650
    • 614650
    • 672055
    • 673656
    • 673662
    • 674655
    • 674668
    • 674669
    • 716154
    • 762055
    • 763656
    • 763662
    • 765100
    • 765559
    • 772055
    • 773656
    • 773662
    • 775100
    • 775659
    • 776150
Amount recalled
146,944,334 units

Where it was sold

Why it was recalled

The potential for air appearing in the enteral feed pumping set tubing during set-up.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Cardinal Health 200, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:46 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.