BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    M POWER PRO 6202

    MDR report key: 2142461 · Received June 22, 2011

    Report

    Report Number
    MW5021118
    Event Type
    Malfunction
    Date Received
    June 22, 2011
    Date of Event
    June 14, 2011
    Report Date
    June 22, 2011
    Manufacturer
    CONMED LINVATEC HALL
    Product Code
    HWE
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CT, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    USING CONMED LINVATEC HALL MPOWER (B)(4) BATTERY DRIVER (B)(4). PUT K-WIRE INTO DRILL AND WHILE INSERTING K-WIRE INTO THUMB JOINT, OIL BEGAN TO LEAK OUT OF END AND LEAKED INTO SURGICAL SITE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 M POWER PRO 6202 NONE HWE CONMED LINVATEC HALL #003

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR