Halyard 42733Recalls & reported problems
Avanos Medical, Inc. · MIC-KEY G, ISO, KIT, 14FRX2.5CM · 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 10680651427332), received between Nov 20, 2019 and Nov 20, 2019 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 20, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED BY THE PATIENT'S WIFE THAT THE PATIENT DEVELOPED AN INFECTION OUTSIDE OF THE TUBE. HE IS ON ANTIBIOTICS AND THE TUBE IS STILL IN PLACE. THE PATIENT IS DUE TO BE SEEN BY THE NURSE TO CHANGE OUT THE WATER. THE TUBE WAS GIVEN TO THE PATIENT BY A DIETITIAN. NO OTHER INJURIES TO THE PATIENT. PER ADDITIONAL INFORMATION RECEIVED 2019-11-19, THE PATIENT'S CURRENT CONDITION IS UNKNOWN. THE LOT NUMBER OF THE DEVICE IS UNKNOWN.
Patient problems: Unspecified Infection
MAUDE report 9349293 ↗
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- 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
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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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