BEUDAMED
    FDA Adverse Event Injury Summary report: N

    JOHNSON & JOHNSON COMPANY

    MDR report key: 1980196 · Received February 4, 2011

    Report

    Report Number
    MW5019261
    Event Type
    Injury
    Date Received
    February 4, 2011
    Date of Event
    July 29, 2010
    Report Date
    January 10, 2011
    Product Code
    JWH
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    GA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    HAD A DEPUY KNEE REPLACEMENT ON (B)(6) 2010, STARTED HAVING TROUBLE WITH IT ON (B)(6) 2010, STARTED POPPING AND CRACKING WHEN I WOULD GET UP FROM A SITTING POSITION, WOULD ABOUT THROW ME DOWN, HURT, FELT LIKE PINS STICKING IN IT, WAS STIFF AND SORE AND WOULD CAUSE MY FOOT TO GO NUMB.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JOHNSON & JOHNSON COMPANY DEPUY KNEE REPLACEMENT JWH ROTATING PLATFORM KNEE

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Required Intervention| S