CONMED 00502317100Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854006153), received between May 5, 2022 and May 5, 2022 — 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.

• MalfunctionMay 5, 2022Material Fragmentation; Material Fragmentation

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE, 00502317100, 13.5 X 25.5 X 0.4MM MICRO OSCILLATOR BLADE, CRESCENTIC WAS BEING USED ON (B)(6) 2022 DURING AN ANKLE RECONSTRUCTION PROCEDURE AND ¿THE BLADE SNAPPED INTO TWO PIECES WHILE DR (B)(6) MAKING A CUT. NEITHER THE DOCTOR NOR THE PATIENT WAS INJURED; ONE PART OF THE BLADE STAYED IN THE MICROFREE HANDPIECE AND THE OTHER WAS LODGED IN THE BONE.¿ AFTER FURTHER ASSESSMENT IT WAS FOUND THAT THE DEVICE FRAGMENTS WERE COMPLETELY RETRIEVED WITH NEEDLE-NOSE CLAMPS. THE PROCEDURE WAS COMPLETED WITH A 1 MINUTE DELAY WHILE SWAPPING OUT BLADES. THERE WAS NO INJURY OR IMPACT TO THE PATIENT OR USER. 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 14285621 ↗