BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DEPUY KNEE REPLACEMENT

    MDR report key: 3022806 · Received March 21, 2013

    Report

    Report Number
    MW5029481
    Event Type
    Injury
    Date Received
    March 21, 2013
    Date of Event
    June 1, 2008
    Report Date
    March 21, 2013
    Product Code
    JWH
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MS, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD A DEPUY IMPLANT FAILURE. I HAVE HAD 2 REVISION. THE DEPUY KNEE IMPLANT CAUSED DAMAGES, SCAR TISSUE, BONY FRAGMENTS, SWELLING AND DISFIGUREMENT OF MY THERAPY FOR 3 YEARS AND I AM STILL UNDER A KNEE DOCTORS CARE. DEPUY JOHNSON AND JOHNSON KNEE REPLACEMENT THERAPY FOR 3 YEARS PLUS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    118413 DEPUY KNEE REPLACEMENT DEPUY JOHNSON & JOHNSON JWH

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR Other| S