Captura G56055Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00827002560550), received between Jul 7, 2017 and Jul 7, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Misassembled During Manufacturing /Shipping” (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 16, 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.

• MalfunctionJul 7, 2017Device Misassembled During Manufacturing /Shipping; Device Operates Differently Than Expected; Device Misassembled During Manufacturing /Shipping; Device Operates Differently Than Expected

  DURING AN COLONOSCOPY , THE PHYSICIAN USED A COOK CAPTURA SERRATED MAX FORCEPS-SPIKE. DURING A BIOPSY, THE OPERATOR HEARD A SNAP IN THE HANDLE AND THE DEVICE WOULD NO LONGER CLOSE. A NEW DEVICE WAS OPENED TO COMPLETE THE PROCEDURE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 6693009 ↗