Halyard 94784Recalls & reported problems
Avanos Medical, Inc. · HALYARD* MIC* G Feeding Tube, Stock# 0100-24 · 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10680651947847), received between Nov 1, 2017 and Nov 1, 2017 — classified as 1 injury.
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
- Injury1
- No Code Available1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 1, 2017Leak/Splash; Leak/Splash
IT WAS REPORTED TO THE DOCTOR BY THE PATIENT'S WIFE THAT THE FEEDING TUBE WAS PULLED ON BY ACCIDENT, AND THE STOMA SITE BECAME PAINFUL. UPON EXAMINATION BY THE DOCTOR, IT APPEARED THAT THE SILICONE INNER RING HAD BECOME INVERTED, AND WAS LYING INSIDE THE STOMA TRACT. THE SUTURES FROM THE MINI LAPAROTOMY PERFORMED 10 DAYS PRIOR TO PLACE THE DEVICE HAD COME LOOSE AND WERE VISIBLE UNDERNEATH THE SILICONE RING. THE BALLOON WAS FOUND TO BE EMPTY. AN ATTEMPT WAS MADE TO REFILL THE BALLOON WITH 10 ML WATER, BUT AFTER ONE MINUTE THERE WAS NO WATER PRESENT IN THE BALLOON. THE PATIENT WAS ADVISED TO SEEK HOSPITALIZATION. NO FURTHER INFORMATION AVAILABLE AT THIS TIME.
Patient problems: Injury; No Code Available; Pain
MAUDE report 6993705 ↗
Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices
- Bard® DigniShield® Stool Management System SMS002C. R. Bard, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 deaths525 reports
- CORTRAK* 2 ENTERAL ACCESS SYSTEM 20-0950Avanos Medical, Inc. · Tubes, gastrointestinal (and accessories)1 recall22 deaths134 reports
- Bard Tri-Funnel Replacement Gastrostomy Tube 000720Bard Access Systems, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 death170 reports
- EndoVive Safety PEG Kit M00566470Boston Scientific Corporation · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 recall1 death111 reports
- Kangaroo 8884711253Cardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)152 reports
- NutraGlide Nasal Feeding Tube ENFT-05055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-06055-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page