CORFLO Enteral Feeding Tube 42-1365Recalls & reported problems
Corpak Medsystems, Inc. · Feeding Tube with ENFit Connectors non weighted · Class 2
All models of CORFLO Enteral Feeding Tube (14)
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 10815149020539), received between Feb 10, 2022 and Feb 10, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Component” (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
- Defective Component1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 10, 2022Defective Component
NOTICEABLE DEFECT IN FEEDING TUBE SHOWED UP ON X-RAY. FIRST THOUGHT TO BE KINK THEN APPEARED TO BE A FRACTURE. ENTERIC TUBE REMOVED, FOUND TO BE INTACT, BUT LARGE WEAK SPOT/BALLOONING NOTED NEAR DISTAL END. A NEW FEEDING TUBE WAS SUBSEQUENTLY PLACED. THIS TUBE WAS IN AN INFANT. PICTURES AVAILABLE UPON REQUEST. THE TUBE COULD HAVE RUPTURED AND PORTION BEEN RETAINED IN THE STOMACH, WHICH WOULD HAVE REQUIRED ENDOSCOPY OR SURGERY FOR RETRIEVAL. AVANOS HAS BEEN CONTACTED REGARDING ISSUE. HAVE NOT RECEIVED RESULTS FROM ANALYSIS YET BUT THERE HAS NOT BEEN ANY ADDITIONAL PRODUCT REPORTS ISSUED ON THIS PRODUCT.
Patient problems: Insufficient Information
MAUDE report 13505575 ↗
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
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-05090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- Kangaroo 8884711253ECardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)100 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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