Halyard 94872Recalls & reported problems
Avanos Medical, Inc. · HALYARD* MIC-KEY* G Feeding Tube-16-5-3.0 · 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 10680651948721), received between May 4, 2017 and May 4, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Collapse” (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
- Collapse1
Patient problems
- Aspiration/Inhalation1
- Pneumonia1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 4, 2017Collapse; Collapse
IT WAS REPORTED BY THE CAREGIVER THAT THE MIC-KEY FEEDING TUBE PLACED ON (B)(6) 2017 COLLAPSED INTERNALLY. THE BALLOON WAS INTACT; HOWEVER, FEEDING BECAME SLOW AFTER A WEEK OR TWO OF PLACEMENT. WHEN TRYING TO VENT THE PATIENT¿S STOMACH THE CAREGIVER USE A PAPER CLIP TO TRY AND UNCLOG THE FEEDING TUBE. THIS DID NOT WORK AND THE PATIENT BEGAN COUGHING AND ASPIRATED. THE PATIENT WAS HOSPITALIZED FROM (B)(6) 2017 FOR ASPIRATION PNEUMONIA. THIS PATIENT WAS SENT HOME FROM THE HOSPITAL WITH ANTIBIOTICS. THE MIC-KEY FEEDING DEVICE WAS REPLACED (B)(6) 2017. CURRENTLY THE PATIENT IS IN STABLE CONDITION AND WELL. NO LONGER TAKING ANTIBIOTICS. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Aspiration/Inhalation; Pneumonia
MAUDE report 6546333 ↗
Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices
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- 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.
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