BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    QUIKDRIVE BATTERY POWERED SCREWDRIVER MINI

    MDR report key: 2121955 · Received May 23, 2011

    Report

    Report Number
    8010177-2011-00144
    Event Type
    Malfunction
    Date Received
    May 23, 2011
    Date of Event
    May 2, 2011
    Report Date
    May 2, 2011
    Manufacturer
    STRYKER OSTEOSYNTHESIS FREIBURG
    Product Code
    LXH
    PMA / PMN Number
    EXEMPT
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION IN PROCESS BUT NOT YET COMPLETE.

    Description of Event or Problem · 1

    QUICK DRIVE MINI IS NOT FUNCTIONING PROPERLY - WHEN A NEW BATTERY WAS PLACED ON IT, IT STARTED SPINNING WITHOUT PUSHING ANY BUTTONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUIKDRIVE BATTERY POWERED SCREWDRIVER MINI INSTRUMENT LXH STRYKER OSTEOSYNTHESIS FREIBURG NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK