Halyard 46017Recalls & reported problems
Avanos Medical, Inc. · HALYARD* CORFLO* Nasogastric/Nasointestinal Feeding Tube with ENFit® Connector and Stylet · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10680651460179), received between Dec 13, 2019 and Dec 13, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (2 reports).
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
- Physical Resistance/Sticking2
Patient problems
- No Consequences Or Impact To Patient1
- Sedation1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 13, 2019Physical Resistance/Sticking; Physical Resistance/Sticking
AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWO DIFFERENT EVENTS. THIS IS THE SECOND OF TWO REPORTS. REFER TO 3011270181-2019-00071 FOR THE SECOND EVENT. IT WAS REPORTED WHEN PHYSICIAN TRIED TO REMOVE THE DEVICE, THE TUBE SEEMS TO GET STUCK IN THE SEPTUM. THE PHYSICIAN STATED AS HE WAS REMOVING THE DEVICE, HE ENCOUNTERED RESISTANCE, STOPPED PULLING, AND THEN THE NURSE TRIED. IT WAS JUST STUCK. THE PHYSICIAN HAD TO USE A GLIDE SCOPE AND PULLED THE DEVICE OUT THROUGH THE PATIENT'S MOUTH. THERE WAS NO REPORTED INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9465813 ↗MalfunctionDec 13, 2019Physical Resistance/Sticking; Physical Resistance/Sticking
AVANOS MEDICAL, INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWO DIFFERENT EVENTS. THIS IS THE FIRST OF TWO REPORTS. REFER TO 3011270181-2019-00072 FOR THE SECOND EVENT. IT WAS REPORTED WHEN PHYSICIAN TRIED TO REMOVE THE DEVICE, THE TUBE SEEMS TO GET STUCK IN THE SEPTUM. THE PHYSICIAN HAD TO SEDATE THE PATIENT AND REMOVE THEM FROM THE MOUTH. THE PHYSICIAN STATED AS HE WAS REMOVING THE DEVICE, HE ENCOUNTERED RESISTANCE, STOPPED PULLING, AND THEN THE NURSE TRIED. IT WAS JUST STUCK. THE PHYSICIAN THEN HAD TO SEDATE THE PATIENT, USE A GLIDE SCOPE AND PULLED THE DEVICE OUT THROUGH THE PATIENT'S MOUTH. THERE WAS NO REPORTED INJURY.
Patient problems: Sedation
MAUDE report 9465772 ↗
Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices
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- 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
- Kangaroo 8884711253ECardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)100 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
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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