CORFLO PEG ADAPTOR Repair Kit 50-6112Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10815149021581), received between Aug 22, 2017 and Aug 22, 2017 — classified as 1 injury.

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

Recent adverse event reports

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

• InjuryAug 22, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS INITIALLY REPORTED BY THE PATIENT'S FATHER THAT A PEG ADAPTER SNAPPED INTO TWO PIECES. IT WAS NOTED, THAT AS A RESULT, THE TUBE STAYS OPEN AND EXPOSED FOR CONTAMINATION TO ENTER IN, OR THE STOMACH CAN EMPTY ITSELF UNTIL THE ISSUE IS DISCOVERED. IT WAS NOTED THAT REPORTER BELIEVES THAT BACTERIA WENT IN AND HIS SON BECAME ILL. EXTRA CAUTION WAS NOTED TO BE TAKEN TO PREVENT ADDITIONAL BREAKS. ADDITIONAL INFORMATION RECEIVED ON 25-JUL-2017 FROM THE PATIENT'S FATHER STATED THAT HIS SON BECAME SICK 24 HOURS AFTER A PEG ADAPTER BREAK, WHICH HE BELIEVES CAUSED HIS SON'S CHEST INFECTION. A VISIT TO THE HOSPITAL WAS REQUIRED IN ORDER TO OBTAIN AND ADMINISTER ANTIBIOTICS. THE FATHER NOW USES SELLOTAPE AS A PREVENTATIVE. NO FURTHER INFORMATION WAS RECEIVED.

  Patient problems: Unspecified Infection

  MAUDE report 6811513 ↗