BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STRYKER

    MDR report key: 2142487 · Received June 23, 2011

    Report

    Report Number
    MW5021131
    Event Type
    Injury
    Date Received
    June 23, 2011
    Date of Event
    August 12, 2008
    Report Date
    June 16, 2011
    Manufacturer
    STRYKER
    Product Code
    JWH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    BAD IMPLANT KNEE. HURT ALL TIME. THERAPY: (B)(6) 2008, (B)(6) 2010. IN HOUSE RN, HOSPITAL 6 TIMES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER STRYKER TOTAL KNEE-REPLACEMENT JWH STRYKER

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Disability