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CONMED 00509123800Recalls & reported problems

Conmed Corporation · OVAL BUR, MEDIUM, CARBIDE 5.5 X 10 MM · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854005057), received between Jan 19, 2018 and Jan 19, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

Device problems

  • Break1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 19, 2018Break; Break

    A CUSTOMER REPORTED DURING A SHOULDER PRE-OP, THREE 00509123600 OVAL BURS BROKE. AN ALTERNATIVE BUR WAS USED IN A MICROPOWER PLUS DRILL ON THE PATIENT AND THE PROCEDURE WAS COMPLETED. NO PATIENT INJURY WAS REPORTED. THIS REPORTED IS RAISED ON THE BASIS OF A DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY WITH RECURRENCE.

    Patient problems: No Patient Involvement

    MAUDE report 7207450 ↗

Other BUR, SURGICAL, GENERAL & PLASTIC SURGERY devices

All BUR, SURGICAL, GENERAL & PLASTIC SURGERY devices →

Sources and updates

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