BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MICRO DRILL

    MDR report key: 2233151 · Received July 22, 2011

    Report

    Report Number
    1811755-2011-02643
    Event Type
    Malfunction
    Date Received
    July 22, 2011
    Date of Event
    June 27, 2011
    Report Date
    June 27, 2011
    Manufacturer
    STRYKER INSTRUMENTS KALAMAZOO
    Product Code
    HBE
    PMA / PMN Number
    K032303
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    CORROSION DAMAGE OF THE SOCKET WAS IDENTIFIED AS THE PROBABLE CAUSE OF THE FAILURE.

    Description of Event or Problem · 1

    THE MICRO DRILL WAS SENT IN FOR EVAL BECAUSE IT WOULD NOT STOP RUNNING DURING A PROCEDURE. THE PROCEDURE WAS SUCCESSFULLY COMPLETED; NO ADVERSE CONSEQUENCE WAS ASSOCIATED WITH THE DEVICE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK