BEUDAMED
    FDA Adverse Event Other Summary report: N

    STRYKER INSTRUMENTS

    MDR report key: 751923 · Received August 12, 2005

    Report

    Report Number
    MW1036330
    Event Type
    Other
    Date Received
    August 12, 2005
    Date of Event
    July 19, 2005
    Report Date
    August 12, 2005
    Manufacturer
    STRYKER INSTRUMENTS
    Product Code
    HTW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IN THE MIDDLE OF THE CASE THE STRYKER DRILL SYSTEM DID NOT WORK. IT HAD WORKED AT THE BEGINNING OF THE CASE, BUT FAILED AFTER INITIATION OF THE CASE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER INSTRUMENTS STRYKER HAND-HELD DRILL HTW STRYKER INSTRUMENTS 4103 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other