AVANOS 44568Recalls & reported problems
Avanos Medical, Inc. · MIC* Jejunal Feeding Tube with ENFit® Connector · Class 2 · Implant
- 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 00350770445687), received between Feb 13, 2024 and Feb 13, 2024 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 13, 2024Break; Break
IT WAS REPORTED VIA FDA VOLUNTARY MEDWATCH REPORT MW5149698, ¿ON (B)(6) 2023, AN AVANOS MIC JEJUNAL FEEDING TUBE WAS PLACED USING DIVINCI LAPAROSCOPIC DEVICE. ON (B)(6) 2023, A CT (COMPUTED TOMOGRAPHY) SCAN WAS ORDERED FOR FOLLOW UP ON ANOTHER UNRELATED PROCEDURE. AN OBJECT WAS IDENTIFIED TO BE IN HIS PELVIS AND THE SURGEON OPTED TO TAKE THE PATIENT TO THE OR (OPERATING ROOM) FOR A POSSIBLE RETAINED FOREIGN OBJECT. A DIAGNOSTIC LAPAROSCOPY WAS PERFORMED AND A CLEAR PIECE OF TUBING WAS REMOVED. THE TUBING WAS NOTED TO BE A PORTION OF THE AVANOS MIC JEJUNAL FEEDING TUBE THAT WAS PLACED ON (B)(6) 2023 THAT APPARENTLY BROKE OFF DURING THE PROCEDURE. THE REMAINING PORTION OF THE J-TUBE WAS IN PLACE.¿
Patient problems: Foreign Body In Patient
MAUDE report 18699643 ↗
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.