Centra 00711249Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00724995180638), received between Jun 17, 2024 and Jun 17, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Use of Device Problem” (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.

• MalfunctionJun 17, 2024Use of Device Problem; Use of Device Problem

  THE USER FACILITY REPORTED TWO INSTANCES OF POST BIOPSY BLEEDING FOLLOWING USE OF THE CENTRA BIOPSY FORCEPS. THE FIRST PATIENT WAS TREATED WITH HEMOCLIPS DURING THE PROCEDURE, CAUSING A PROCEDURE DELAY. THE SECOND PATIENT WAS TREATED DAYS LATER WITH NO ADDITIONAL ENDOSCOPY. THE USER FACILITY ALSO REPORTED DIFFICULTY PASSING THE CENTRA BIOPSY FORCEPS THROUGH THE ENDOSCOPE CHANNEL.

  Patient problems: Laceration(s)

  MAUDE report 19553612 ↗