Halyard 46032Recalls & reported problems
Avanos Medical, Inc. · HALYARD* CORFLO* Nasogastric/Nasointestinal Feeding Tube with ENFit® Connector and Stylet · Class 2
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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10680651460322), received between Apr 23, 2020 and Apr 23, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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
- Material Deformation1
- Material Rupture1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 23, 2020Material Rupture; Material Deformation; Material Rupture; Material Deformation
IT WAS REPORTED THAT THE DEVICE WAS "PLACED ON (B)(6) 2020, RUPTURED ON (B)(6) 2020. TUBE NOTED TO BE CLOGGED ON (B)(6) 2020, ATTEMPTED CLOG ZAPPER WITH NO IMPROVEMENT, KUB [KIDNEY, URETER, BLADDER X-RAY] SHOWED KINK, PULLED BACK TUBE 2 CM, CLOG ZAPPER AGAIN, THEN FLUSHED, (B)(6) 2020 PINK COLORING OF ETT [ENDOTRACHEAL TUBE] SECRETIONS WHICH MATCHED MEDS PREV. GIVEN VIA TUBE." "KUB FINDINGS: LIKELY SMALL KINK IN THE REGION THE PROXIMAL GASTRIC PORTION OF THE ENTERIC TUBE." "(B)(6) 2020 UNCHANGED FEEDING TUBE OPENING AT DISTAL DUODENUM WITH KINK IN GASTRIC PORTION OF TUBING." "(B)(6) 2020 CONTINUED FOCAL KINKING IN THE PROXIMAL GASTRIC PORTION OF THE ENTERIC TUBE." PATIENT WAS NOT REPORTED TO BE INJURED. ADDITIONAL INFORMATION RECEIVED ON 02-APR-2020 INDICATED "A KINK AT THE 25CM MARKING-ALSO THE TUBE DISPLAYS A BREAK ABOVE THE SITE OF THE KINK- IT IS IN TWO PIECES-THE DISTAL PORTION WAS RETRIEVED VIA ENDOSCOPY ON (B)(6) 2020." NO ADVERSE EFFECTS WERE REPORTED. CUSTOMER REPORTED THAT "TUBE IN FOR GREATER THAN 30 DAY AND THAT STAFF MAY HAVE USED FORCE IN AN ATTEMPT TO DE-CLOG."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9990407 ↗
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