CORFLO PEG Kit 30-5020Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10815149024087), received between Apr 3, 2017 and Apr 3, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Collapse” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryApr 3, 2017Collapse; Collapse

  A REPORT WAS RECEIVED STATING THE PATIENT HAD THE TUBE PLACED ON (B)(6) 2017. THE PATIENT HAD AN ABDOMINAL X-RAY ON (B)(6) 2017 (5 DAYS LATER). THE X-RAY REVEALED FLUID IN THE PATIENT'S ABDOMEN AND THE PATIENT WAS THEN TAKEN BACK TO THE OPERATING ROOM (OR). THE BUMPER OF THE TUBE WAS COMPLETELY WAS NO LONGER POSITIONED IN THE STOMACH. THE SURGEON REPAIRED THE STOMACH. WHEN ASKED WHAT PROCEDURE THE SURGEON PERFORMED IT WAS NOTED TO BE A GASTROSTOMY WITH PLACEMENT OF A GASTROSTOMY TUBE. THE SURGEON "BASICALLY SUTURED THE HOLE AND PLACED ANOTHER TUBE DOWN LOWER TO ALLOW THE STOMACH TO HEAL." WHEN ASKED THE PATIENT'S CURRENT STATUS IT WAS NOTED, "THE PATIENT IS VERY SICK IN ICU." IT COULD NOT BE CONFIRMED IF THE PATIENT WAS IN THE ICU BEFORE THIS PROCEDURE AND CLINICIAN STATED SHE BELIEVES SO BECAUSE THE PATIENT HAS BEEN IN AND OUT OF THE ICU LATELY HAD A LOT OF COMORBIDITIES. HOWEVER, THE CLINICIAN COULD NOT BE CERTAIN. THE PATIENT ALSO HAD A TRACHEOSTOMY TUBE PLACED ON THE SAME DAY OF THE (B)(6) 2017 PROCEDURE.

  Patient problems: Peritonitis

  MAUDE report 6454079 ↗