AVANOS 44099Recalls & reported problems
Avanos Medical, Inc. · MIC-KEY* Gastric-Jejunal Feeding Tube Kit Extension Sets · Class 2 · Implant
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00350770440996), received between Apr 8, 2026 and Apr 24, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Complete Blockage” (2 reports).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- May 31, 2024Open, Classified
The IFU was missing some risk information requested by another country to be contained in the IFU pertaining to potential complications.
Z-2422-2024 · Root cause: Error in labeling · FDA record ↗
Most reported problems
Device problems
- Complete Blockage2
- Break1
- Fluid/Blood Leak1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Vomiting1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 24, 2026Break; Complete Blockage
IT WAS REPORTED THAT THERE WAS RESISTANCE WHEN FLUSHING AN NG TUBE. THEN ALL OF THE SUDDEN THE RESISTANCE WAS GONE. NO VOMITING BUT AGAIN, THEY COULD ASPIRATE FEED FROM GASTRIC PORT. LEAK INTO STOMACH CONFIRMED WHEN INJECTING CONTRAST INTO THE JEJUNAL LIMB UNDER X-RAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24982902 ↗InjuryApr 8, 2026Complete Blockage; Fluid/Blood Leak
IT WAS REPORTED THAT A PATIENT STARTED VOMITING FEED. THEY WERE ABLE TO ASPIRATE FEED WHICH WAS GIVEN VIA JEJUNAL PORT FROM THE GASTRIC PORT. UPON INJECTION OF THE JEJUNAL PORT UNDER X-RAY, THERE WAS CONTRAST LEAKAGE AROUND THE STOMA SITE AND INTO THE STOMACH IN KEEPING WITH JEJUNAL LIMB FRACTURE. MUM DESCRIBES ISSUES OCCURRED AFTER FORCEFULLY FLUSHING A TUBE BLOCKAGE.
Patient problems: Vomiting
MAUDE report 24821135 ↗
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.