BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STRYKER CORPORATION

    MDR report key: 1226187 · Received November 8, 2008

    Report

    Report Number
    MW5008932
    Event Type
    Injury
    Date Received
    November 8, 2008
    Date of Event
    October 19, 2007
    Report Date
    November 8, 2008
    Manufacturer
    STRYKER CORPORATION
    Product Code
    JDI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    IN 2007, I HAD A "STRYKER CORPORATION DEVICE HIP REPLACEMENT". MY RIGHT HIP. IN APPROX THREE MONTHS LATER, IT WAS FOUND "DEFECTIVE" REQUIRING A REVISION. THE REVISION CONSISTED OF 2 SCREWS BEING INSERTED IN THE DEVICE THROUGH TO MY HIP. I AM UNABLE TO SIT ON A FIRM CHAIR OR LIE ON MY RIGHT SIDE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER CORPORATION HIP REPLACEMENT JDI STRYKER CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention