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Kangaroo 8884741220Recalls & reported problems

Cardinal Health, Inc. · True content to be populated as part of rebranding · Class 2 · Implant

All models of Kangaroo (145)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521011526), received between May 3, 2018 and May 3, 2018 — classified as 1 malfunction.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 3, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    THE CUSTOMER STATED THAT THE TUBE WAS BROKEN WHEN OPENED BY THE RADIOLOGIST BEFORE PUTTING INTO PATIENT, PRIOR TO PRIMING.

    Patient problems: No Patient Involvement

    MAUDE report 7483631 ↗

Other Tubes, Gastrointestinal (And Accessories) devices

All Tubes, Gastrointestinal (And Accessories) devices →

Sources and updates

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