CONMED 00507112400Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854000328), received between Mar 20, 2024 and Mar 20, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Fragmentation” (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.

• MalfunctionMar 20, 2024Material Fragmentation; Material Fragmentation

  THE CUSTOMER REPORTED THAT 00507112400, 25.4 X 95 X 1.27MM (.050INCH) OSCILLATOR BLADE, 5 EA, WAS BEING USED DURING A HIP PROSTHESIS PROCEDURE ON (B)(6) 2024 WHEN IT WAS REPORTED "ONE OF THE TOOTH OF THE BLADE BROKE WHILE ENGRAVING THE BONE. BROKEN PIECE FALLEN INTO THE OPERATORY FIELD BUT COMPLETELY REMOVED." THERE WAS NO REPORT OF INJURY, MEDICAL INTERVENTION, OR PROLONGED HOSPITALIZATION FOR THE PATIENT. THIS REPORT IS BEING RAISED ON THE BASIS OF MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18940250 ↗