AVANOS 42-9558Recalls & reported problems
Avanos Medical, Inc. · CORFLO* Nasogastric/Nasointestinal Feeding Tube with Stylet with ENFit® Connector · Class 2
- 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 00350770460994), received between Dec 29, 2021 and Dec 5, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Fragmentation” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Material Fragmentation1
- Material Rupture1
- Obstruction of Flow1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 5, 2023Material Rupture; Obstruction of Flow; Material Rupture; Obstruction of Flow
IT WAS REPORTED, UNABLE TO FLUSH NASOJEJUNAL TUBE (NJT). APPLIED MORE PRESSURE AND NJT POPPED AND RIPPED APART FROM THE BRIDLE POINT. IV FLUID PRESCRIBED AND COMMENCED. NO INJURY REPORTED. PER ADDITIONAL INFORMATION RECEIVED ON 13NOV2023, IT IS UNKNOWN IF ANY PORTION OF THE TUBE WAS RETAINED INSIDE THE PATIENT AND IT IS UNKNOWN IF ANY PORTION OF THE TUBE HAD TO BE REMOVED. THERE WAS NO MEDICAL INTERVENTIONS REQUIRED. THE PATIENT¿S CONDITION WAS REPORTED TO BE STABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18266956 ↗MalfunctionDec 29, 2021Material Fragmentation; Material Fragmentation
IT WAS REPORTED THAT WHEN THE NASAL-JEJUNAL TUBE WAS REMOVED, THE TIP WAS NOTED TO BE MISSING. THE DEVICE HAD BEEN PLACED ON (B)(6) 2021 UNDER VIDEO FLUROSCOPY. PER ADDITIONAL INFORMATION RECEIVED 17 DEC 2021, THE PATIENT'S CONDITION IS OK AND NO MEDICAL INTERVENTION WAS REQUIRED. PER ADDITIONAL INFORMATION RECEIVED 20 DEC 2021, THE REPORTER CONFIRMED THAT THE TIP WAS NOT REMOVED FROM THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13109034 ↗
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.