BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MIKA KNEE INSTRUMENT

    MDR report key: 2091152 · Received May 10, 2011

    Report

    Report Number
    1644408-2011-00264
    Event Type
    Malfunction
    Date Received
    May 10, 2011
    Date of Event
    May 2, 2011
    Report Date
    May 2, 2011
    Manufacturer
    ENCORE MEDICAL, L.P.
    Product Code
    LXH
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    INSTRUMENT FAILURE - THE MIKA RESECTION GUIDE IS WORN AND THE DISTAL FEMORAL CUT BLOCK IS STICKING TO IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MIKA KNEE INSTRUMENT DISTAL FEMORAL CUT GUIDE LXH ENCORE MEDICAL, L.P. 37990108

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR