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Kangaroo 8884752042Recalls & reported problems

Cardinal Health, Inc. · Y-Port/PEG Adapter,Yellow · Class 2 · Implant

Data updated Oct 13, 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 10884521518995), received between Sep 21, 2022 and Sep 21, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (1 report).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Fluid/Blood Leak1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionSep 21, 2022Fluid/Blood Leak; Fluid/Blood Leak

    PATIENT USER OF GASTROSTOMY, STATES THAT SINCE CHANGING THE CONNECTOR THERE IS A LEAK OF THE NUTRITION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15461093 ↗

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

All TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices →

Sources and updates

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