SiL Feeding Tube FTM6.5S-EORecalls & reported problems
Avanos Medical, Inc. · SIL Feeding Tube Orange 6.5Fr 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 00350770002125), received between Nov 30, 2022 and Dec 7, 2022 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Integrity Problem” (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.
Most reported problems
Device problems
- Material Integrity Problem1
- Material Split, Cut or Torn1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 7, 2022Material Integrity Problem; Material Integrity Problem
IT WAS REPORTED, WHEN THE NEONATE INTENSIVE CARE UNIT (NICU) NURSE REMOVED THE FEEDING TUBE FROM THE BABY THEY NOTED THE TUBE WAS BROKEN OFF. THERE WAS NO REPORTED INJURY.
Patient problems: Foreign Body In Patient
MAUDE report 15932659 ↗MalfunctionNov 30, 2022Material Split, Cut or Torn; Material Split, Cut or Torn
IT WAS REPORTED, THE FEEDING TUBE WAS FOUND SPLIT WHILE REMOVING IT FROM THE NICU PATIENT. THERE WAS NO REPORTED INJURY TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15890796 ↗
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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