CORFLO ULTRA Lite NG Feeding Tube 20-9368Recalls & reported problems
Corpak Medsystems, Inc. · Feeding tube, non weighted, with stylet · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10815149023868), received between Feb 24, 2017 and Feb 24, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Material Perforation” (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 Perforation1
Patient problems
- Abdominal Distention1
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 24, 2017Material Perforation; Material Perforation
AN FDA MEDWATCH REPORT,(B)(4) WAS RECEIVED STATING, "EVENT DESC: A CORTRAK NASOGASTRIC JEJUNAL TUBE (NGT) WAS INSERTED IN A PATIENT AND PLACEMENT WAS RADIOLOGICALLY CONFIRMED AT THE DUODENAL AREA. PEDIATRIC SURGERY WAS CONSULTED 5 DAYS LATER FOR ABDOMINAL DISTENTION AND SUSPICION FOR NECROTIZING ENTERCOLITIS (NEC). THE PATIENT SUBSEQUENTLY UNDERWENT ABDOMINAL EXPLORATORY LAPAROTOMY THE FOLLOWING DAY WITH FINDINGS JEJUNAL PERFORATION LOCATED AT THE DISTAL TIP OF THE NASOGASTRIC NJ TUBE." ADDITIONAL INFORMATION RECEIVED 31-JAN-2017 DETAILING AGE, WEIGHT ((B)(6)) AND GENDER.
Patient problems: Abdominal Distention; No Code Available
MAUDE report 6357784 ↗
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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