Skip to content

CORFLO PEG Kit 50-6016Recalls & reported problems

Corpak Medsystems, Inc. · PEG Kit with ENFit Connectors Pull Technique · Class 2 · Implant

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 10815149021550), received between Aug 22, 2019 and Aug 22, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionAug 22, 2019Detachment of Device or Device Component; Detachment of Device or Device Component

    IT WAS REPORTED THAT THE DEVICE "DISPLACED WITHOUT INTERNAL BUMPER. INTERNAL BUMPER THEREFORE RETAINED." ADDITIONAL INFORMATION RECEIVED INDICATED NO INJURIES REPORTED, BUT MEDICAL INTERVENTION WAS REQUIRED TO OBTAIN PART OF THE DEVICE. REQUIRED TUBE REPLACEMENT. FURTHER ADDITIONAL INFORMATION HAS BEEN REQUESTED BUT NOT YET RECEIVED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8922157 ↗

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

All TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.