AVANOS 20-2438Recalls & reported problems
Avanos Medical, Inc. · CORFLO* Nasogastric/Nasointestinal Feeding Tube with Stylet · Class 2
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 00350770457284), received between Jul 1, 2025 and Jul 1, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
- Obstruction of Flow1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 1, 2025Break; Obstruction of Flow; Break; Obstruction of Flow
IT WAS REPORTED VIA MAUDE ADVERSE EVENT REPORT NUMBER (B)(4), ¿KEO FLUSHED APPROPRIATELY BEFORE MEDICATION ADMINISTRATION. PATIENT'S (PT) LAST MEDICATION TO GIVE THROUGH KEO WAS METAMUCIL. METAMUCIL WAS DISSOLVED AND MIXED THOROUGHLY WITH WATER PRIOR TO ADMINISTERING. WHILE USING SYRINGE TO ADMINISTER METAMUCIL, RN (REGISTERED NURSE) WAS UNABLE TO PUSH ENTIRE CONTENTS OF MEDICATION THROUGH KEO AND MET RESISTANCE. AFTER SUCH, ANOTHER SYRINGE OF WATER WAS USED TO ATTEMPT TO FLUSH CONTENTS OF TUBE. AFTER NOT WORKING AND STILL MEETING RESISTANCE, A 6ML SYRINGE WAS USED TO FLUSH THE TUBE IN ORDER TO FURTHER DISSOLVE THE METAMUCIL STUCK IN THE TUBE. AFTER ATTEMPTING SUCH, KEO HAD RIPPED INTO TWO SEPARATE PIECES AND RN SUCTIONED PT ORALLY AND THROUGH TRACH IMMEDIATELY TO MAINTAIN AIRWAY.¿
Patient problems: Insufficient Information
MAUDE report 22372692 ↗
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.
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