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STERLING, MICROBLADE C9940Recalls & reported problems

Conmed Corporation · STERLING FULL RADIUS RESECTOR, MICROBLADE SHAVER, 2.0 MM · Class 1

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 10845854017739), received between Mar 27, 2019 and Mar 27, 2019 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionMar 27, 2019Break; Break

    THE CUSTOMER REPORTED THAT THE C9940, 2.0MM STERLING BUR, DURING THE SURGERY, TIP OF THE INNER SHAFT OF THIS PRODUCT WAS BROKEN. THE TIP WAS RETRIEVED. PICTURES WERE PROVIDED. THERE WAS NO PATIENT INJURY OR DELAY OF SURGERY REPORTED. THIS REPORT IS BEING RAISED BASED ON DEVICE MALFUNCTION WITH POTENTIAL FOR INJURY UPON REOCCURRENCE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8457222 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.