CONMED 00502313800Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854001974), received between Mar 22, 2018 and Mar 22, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Dull, Blunt” (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 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.

• InjuryMar 22, 2018Dull, Blunt; Dull, Blunt

  IT WAS REPORTED BY A CONMED COUNTRY CONTACT ON BEHALF OF THE FACILITY THAT THE (B)(4)BLADE WAS DULL DURING A HALLUX PROCEDURE. THE ISSUE REPEATED WITH 4 BLADES OF THE SAME LOT DURING THE PROCEDURE WHICH ALLEGEDLY CAUSED "DAMAGE TO THE BONE". TO DATE ADDITIONAL INFORMATION REGARDING THE PATIENT STATUS AND PROCEDURE HAS NOT BEEN MADE AVAILABLE ALTHOUGH A REQUEST HAS BEEN MADE TO THE USER FACILITY. ALTHOUGH NO INJURY TO PATIENT OR USER WAS REPORTED, THIS REPORT IS BEING RAISED AS AN INJURY DUE TO THE STATEMENT FROM THE USER OF "DAMAGE TO THE BONE" CAUSED BY A MALFUNCTION OF THE DEVICE.

  Patient problems: Injury

  MAUDE report 7363707 ↗