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Halyard 94776Recalls & reported problems

Avanos Medical, Inc. · HALYARD* MIC* G Feeding Tube, Stock# 0100-18 · 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
1
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10680651947762), received between Mar 22, 2017 and Mar 22, 2017 — classified as 1 death.

The most frequently reported specific device problem is “Leak/Splash” (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

  • Leak/Splash1

Patient problems

  • Abdominal Distention1
  • Bowel Perforation1
  • Death1
  • Diaphoresis1
  • No Code Available1

Recent adverse event reports

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

  • DeathMar 22, 2017Leak/Splash; Leak/Splash

    IT WAS REPORTED BY THE CAREGIVER THAT THE PATIENT DIED (B)(6) 2016. THE PATIENT WAS ADMITTED TO THE HOSPITAL AT THE END OF (B)(6) 2016 FROM THE EMERGENCY ROOM WITH DIAPHORESIS AND A DISTENDED ABDOMEN. THE HOSPITAL PLACED A 22 FRENCH MIC GASTROSTOMY TUBE IN THE PATIENT. TWENTY-FOUR HOURS AFTER PLACEMENT, THE CAREGIVER NOTICED THE STOMA SITE WAS INCREASING IN SIZE. THE PATIENT WAS TRANSFERRED TO A DIFFERENT HOSPITAL AT THE REQUEST OF THE CAREGIVER. DURING TRANSPORT, THE PATIENT HAD EXCESSIVE LEAKING OF GASTRIC CONTENTS AND BLOOD. UPON ARRIVAL AT THE HOSPITAL, THE 22 FRENCH WAS EXPELLED BECAUSE OF A BALLOON BREAK. THE MIC GASTROSTOMY TUBE WAS REPLACED WITH AN 18 FRENCH MIC GASTROSTOMY TUBE. THE CAREGIVER STATED THAT WITHIN 24-HOURS, THE 18 FRENCH MIC GASTROSTOMY TUBE WAS ALSO EXPELLED AND APPEARED INTACT. THE CAREGIVER STATED THE PATIENT EXPERIENCED MULTIPLE SURGERIES, BOWEL LEAKAGE, AND A STOMA SITE FISTULA, 8-INCHES IN DIAMETER. THE PATIENT ALSO RECEIVED BLOOD TRANSFUSIONS DURING THE HOSPITAL STAY, AND WAS RELEASED HOME ON A VENTILATOR. THE PATIENT WAS AT HOME FOR EIGHT TO NINE DAYS AND EXPERIENCED A PERFORATED BOWEL AND WAS RE-ADMITTED TO THE HOSPITAL. ADDITIONAL INFORMATION WAS RE

    Patient problems: Abdominal Distention; Bowel Perforation; Death; Diaphoresis; No Code Available

    MAUDE report 6424808 ↗

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Sources and updates

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