AVANOS 42-1225Recalls & reported problems
Avanos Medical, Inc. · CORFLO* Nasogastric/Nasointestinal Feeding Tube with ENFit® Connector · Class 2
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00350770460734), received between Dec 30, 2025 and Jun 18, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Complete Blockage” (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.
Reports received per month
Most reported problems
Device problems
- Complete Blockage2
- Fluid/Blood Leak2
- Material Puncture/Hole1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Feeding Problem1
- Insufficient Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 18, 2026Complete Blockage
AVANOS MEDICAL INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENTS, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWO DIFFERENT PATIENTS. THIS IS THE FIRST OF TWO REPORTS. REFER TO 9611594-2026-00468 FOR THE SECOND REPORT. IT WAS REPORTED THAT A NASOGASTRIC TUBE WAS OCCLUDED DURING INITIAL USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25552628 ↗MalfunctionJun 18, 2026Complete Blockage
AVANOS MEDICAL INC. RECEIVED A SINGLE REPORT THAT REFERENCED TWO DIFFERENT INCIDENTS, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING TWO DIFFERENT PATIENTS. THIS IS THE SECOND OF TWO REPORTS. REFER TO 9611594-2026-00467 FOR THE FIRST REPORT REFER TO . IT WAS REPORTED THAT A NASOGASTRIC TUBE WAS OCCLUDED DURING INITIAL USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25552626 ↗MalfunctionFeb 19, 2026Fluid/Blood Leak; Material Puncture/Hole
IT WAS REPORTED, "DURING 1630 HANDS ON CARE, RN NOTICED MEDICATION & MILK LEAKING OUT OF OG [OROGASTRIC] TUBE. HOLE FOUND IN TUBING. TUBE REPLACED AND OLD TUBE GIVEN TO SUPERVISOR."
Patient problems: Insufficient Information
MAUDE report 24391192 ↗MalfunctionDec 30, 2025Fluid/Blood Leak; Fluid/Blood Leak
IT WAS REPORTED, "ROUNDED ON PATIENT AND REALIZED THAT THE SHEETS WERE SOILED WITH A SIGNIFICANT AMOUNT OF FEED. I EXAMINED THE FEEDING TUBE AND FLUSHED WITH STERILE WATER TO LOCATE THE LEAK IN IT. I THEN DISCUSSED THE NEXT STEPS WITH THE CARE TEAM, AFTER CHECKING A SUGAR. POINT OF CARE BLOOD SUGAR WAS CHECKED AND THE NEXT FEED WAS STARTED AN HOUR EARLY, AFTER REPLACING THE FEEDING TUBE.¿
Patient problems: Feeding Problem
MAUDE report 23927496 ↗
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
- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.