BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CORE IMPACTION DRILL

    MDR report key: 3073490 · Received April 23, 2013

    Report

    Report Number
    0001811755-2013-00878
    Event Type
    Malfunction
    Date Received
    April 23, 2013
    Date of Event
    April 4, 2013
    Report Date
    April 4, 2013
    Manufacturer
    STRYKER INSTRUMENTS-KALAMAZOO
    Product Code
    DZJ
    PMA / PMN Number
    K040369
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON DISASSEMBLY FOR VISUAL INSPECTION, CORROSION WAS FOUND TO BE BUILT UP THROUGHOUT THE INSIDE OF THE HANDPIECE.

    Description of Event or Problem · 1

    IT WAS REPORTED DURING TESTING THAT THE CORE IMPACTION DRILL CONTINUED TO RUN WHEN THE TRIGGER WAS NO LONGER ACTIVATED. THERE WAS NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCE ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    174322 CORE IMPACTION DRILL DRIVER, WIRE, AND BONE DRILL, DZJ STRYKER INSTRUMENTS-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1