AVANOS 44566Recalls & reported problems
Avanos Medical, Inc. · MIC* Jejunal Feeding Tube with ENFit® Connector · Class 2 · Implant
Data updated Oct 13, 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 00350770445663), received between Mar 9, 2020 and Mar 9, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Migration” (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.
Most reported problems
Device problems
- Migration1
Patient problems
- Increased Respiratory Rate1
- Pain1
- Sweating1
- Tachycardia1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 9, 2020Migration; Migration
FDA MEDWATCH / FDA USER FACILITY REPORT # (B)(4) RECEIVED ON 17-FEB -2020, AND THE FOLLOWING INFORMATION WAS PROVIDED: "DESCRIBE THE EVENT OR PROBLEM: PATIENT HAD A JEJUNOSTOMY TUBE (J-TUBE) REQUIRING CARDIZEM MEDICATION TO BE INSTILLED AT 0026, TUBE FEEDING MACHINE WAS PAUSED, WHAT APPEARED TO BE "PORT" OF TUBE FEEDING LINE HAD 20ML WATER FLUSHED THROUGH, AND HALF OF CRUSHED CARDIZEM MED IN WATER WAS ADMINISTERED. LINE BEGAN TO GET SLUGGISH AND THEN A POP SOUND OCCURRED AT THIS POINT PATIENT COMPLAINED OF SHARP PAIN. DOCTOR AND CHARGE NURSE WERE NOTIFIED DOCTOR SAID TO TURN OFF TUBE FEEDING FOR THE TIME BEING, AND ATTEMPT INSTILLING SECOND HALF OF CARDIZEM MEDICATION AT 0200 AT 0200, THE CARDIZEM MEDICATION AGAIN WOULD NOT GO INTO THE J-TUBE, AND WITH JUST ABOUT 3ML OF CONTENT ADMINISTERED THE PATIENT AGAIN COMPLAINED OF SHARP PAIN, SO I STOPPED ALL MED ADMINISTRATION I ASKED FOR A SECOND OPINION ON THE PATIENT'S STATUS AND NOTIFIED THE CRISIS NURSE WE CHANGED THE WOUND DRESSING AT THE SITE NURSE ASSESSMENT AND MINE ALSO WARRANTED NOTIFYING THE DOCTOR USING THE "I AM CONCERNED" STATEMENTS, AND DOCTOR CAME TO THE BEDSIDE TO ALSO SEE HOW THE PATIENT WAS DOING. THE PATIENT'S BELLY LO
Patient problems: Increased Respiratory Rate; Pain; Sweating; Tachycardia
MAUDE report 9809180 ↗
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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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