BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MICRO OSCILLATING SAW

    MDR report key: 2140393 · Received June 17, 2011

    Report

    Report Number
    1811755-2011-02237
    Event Type
    Malfunction
    Date Received
    June 17, 2011
    Date of Event
    May 13, 2011
    Report Date
    May 25, 2011
    Manufacturer
    STRYKER INSTRUMENTS KALAMAZOO
    Product Code
    HBE
    PMA / PMN Number
    K032303
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    CORROSION DAMAGE WAS NOTED WITHIN THE INTERNAL COMPONENTS OF THE DEVICE.

    Description of Event or Problem · 1

    THE MICRO OSCILLATING SAW WAS SENT IN FOR EVAL BECAUSE METAL FLAKES WERE COMING OUT OF THE DEVICE DURING A PROCEDURE. METAL FLAKES WERE NOTED IN THE SURGICAL SITE AND WERE SUCCESSFULLY CLEANED OUT. NO MEDICAL TREATMENT WAS REPORTED AS A RESULT OF THIS EVENT. A REPLACEMENT DEVICE WAS READILY AVAILABLE AND IT WAS USED TO COMPLETE THE PROCEDURE WITH A 2 MIN DELAY. NO ADVERSE EVENT WAS ASSOCIATED WITH THE DEVICE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICRO OSCILLATING SAW HBE STRYKER INSTRUMENTS KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK