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Halyard 10229Recalls & reported problems

Avanos Medical, Inc. · HALYARD* Laparoscopic Introducer Kit for Jejunal/Gastric Jejunal Feeding Tube · Class 2

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 10680651102291), received between Mar 27, 2017 and Mar 27, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1

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.

  • MalfunctionMar 27, 2017Break; Break

    IT WAS REPORTED BY THE NURSE THAT, THE T-FASTENER BROKE; HOWEVER, THE PROCEDURE WAS COMPLETED. NO INJURY REPORTED. NO ADDITIONAL INFORMATION PROVIDED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6435898 ↗

Other TUBE, GASTRO-ENTEROSTOMY devices

All TUBE, GASTRO-ENTEROSTOMY devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.