SiL Feeding Tube FTM8.0S-EORecalls & reported problems
Avanos Medical, Inc. · SIL Feeding Tube Orange 8Fr 60cm · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00350770002132), received between Feb 2, 2023 and Feb 6, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Integrity Problem” (2 reports).
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.
Most reported problems
Device problems
- Material Integrity Problem2
Patient problems
- Foreign Body In Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 6, 2023Material Integrity Problem; Material Integrity Problem
IT WAS REPORTED, THE TUBE WAS FOUND SPLIT INSIDE THE PATIENT; THE MEDICAL TEAM RETRIEVED THE REMAINING TUBE FROM THE PATIENT WITHOUT INJURY. THERE WAS NO INJURY REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 16308989 ↗MalfunctionFeb 2, 2023Material Integrity Problem; Material Integrity Problem
IT WAS REPORTED, THE TUBE WAS FOUND SPLIT INSIDE THE PATIENT; THE MEDICAL TEAM RETRIEVED THE REMAINING TUBE FROM THE PATIENT WITHOUT INJURY. THERE WAS NO INJURY REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 16284855 ↗
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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