ENFit SIL Feeding Tube FTL8.0S-NCRecalls & reported problems
Avanos Medical, Inc. · ENFit SIL Feeding Tube Orange 8Fr 90cm · Class 2
Data updated Oct 18, 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 00350770000862), received between Jun 11, 2026 and Jun 11, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
- Leak/Splash1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 11, 2026Fracture; Leak/Splash
IT WAS REPORTED THAT A PATIENT FOUND TO HAVE WHAT APPEARED TO BE FORMULA LEAKING ONTO BLANKET NEAR HER HEAD. IT WAS DISCOVERED THAT FORMULA WAS LEAKING FROM A SMALL TEAR IN THE NASOGASTRIC (NG) TUBING DISTAL TO THE INSERTION SITE. NG WAS REMOVED. THERE WAS NO REPORTED INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25471934 ↗
Other TUBE, FEEDING devices
- Bard® Premature Infant Feeding Tube 0036400C. R. Bard, Inc. · TUBE, FEEDING5 reports
- CORTRAK 2 EAS Electromagnetic Transmitting Stylet and CORFLO Feeding Tube 20-9431TRAK2ACorpak Medsystems, Inc. · TUBE, FEEDING5 reports
- EndoVive Jejunal Feeding Tube M00566350Boston Scientific Corporation · TUBE, FEEDING4 reports
- CORFLO ULTRA Lite NG Feeding Tube 20-9366AIV2Corpak Medsystems, Inc. · TUBE, FEEDING4 reports
- AVANOS 20-9366AIV2Avanos Medical, Inc. · TUBE, FEEDING4 reports
- CORFLO ULTRA NG Feeding Tube 20-7431AIV2Corpak Medsystems, Inc. · TUBE, FEEDING3 reports
- CORTRAK 2 EAS Electromagnetic Transmitting Stylet and CORFLO Feeding Tube 20-9551TRAK2ACorpak Medsystems, Inc. · TUBE, FEEDING2 reports
- Halyard 45758Avanos Medical, Inc. · TUBE, FEEDING2 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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