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Formula 0375940200Recalls & reported problems

Stryker Corporation · [Unhooded 6-Flute Round Bur, Arthroscopic Shaver Blade, Do Not Resterilize, Do Not Use if Package is Damaged, Keep Dry, Keep Away from Sunlight] · Class 1

Data updated Oct 13, 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 07613327054736), received between Mar 27, 2020 and Mar 27, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

  • Device Contamination with Chemical or Other Material1

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.

  • MalfunctionMar 27, 2020Device Contamination with Chemical or Other Material

    DISCOVERED WHAT APPEARS TO BE A HAIR WITHIN THE SEAL OF THE PACKAGING - PART OF CONTAMINANT INSIDE PACKAGING WITH DEVICE AND PART OF CONTAMINANT OUTSIDE THE PACKAGING. PACKAGE NOT OPENED; NO PATIENT EXPOSURE.

    Patient problems: No Patient Involvement

    MAUDE report 9888151 ↗

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Sources and updates

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