Skip to content

Halyard 44091Recalls & reported problems

Avanos Medical, Inc. · MICKEY,LPGJ,ISOKIT,-,16X2.0,1 · Class 2 · Implant

All models of Halyard (232)

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 10680651440911), received between Jun 22, 2018 and Jun 22, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Split” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Split1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionJun 22, 2018Split; Split

    IT WAS REPORTED THAT THE FEEDING TUBE SPLIT INSIDE THE PATIENT, AND THE JEJUNAL FEED IS NOW GETTING INTO THE PATIENT'S STOMACH. NO FURTHER INFORMATION HAS BEEN PROVIDED AT THIS TIME.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7632306 ↗

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

All TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page