BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DEPUY ORTHOPEDICS

    MDR report key: 1002053 · Received February 21, 2008

    Report

    Report Number
    MW5005628
    Event Type
    Injury
    Date Received
    February 21, 2008
    Date of Event
    April 1, 2006
    Report Date
    November 13, 2007
    Manufacturer
    DEPUY
    Product Code
    JWH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    AFTER CALLING THE 800 NUMBER TO GET THE FREE INFORMATION FROM DEPUY ORTHOPEDICS, MY KNEES, ESPECIALLY R, WERE HURTING WORSE. IT GOT SO BAD, IT WAS LIKE A TRIPLE GUNSHOT AT THE KNEE-CAP - LIKE SOMEONE WAS GETTING FISTED EVERY NIGHT TO MAKE OTHER PEOPLES CONDO PAYMENTS. THIS PROBLEM CONTINUES AND THE RESULTS ARE DISABLING. I HAVE NOT YET CONSULTED AN ORTHOPEDIC SURGEON. I ALREADY HAD OSTEOARTHRITIS AND DJD, NOW BOTH THOSE COMPLICATED BY RHEUMATOID, POSSIBLY 20 TO RISPERDAL? CONDO IS POSSIBLY THE LINDELL TERRACE (MAY BE DELL TERR NOW). DOSE OR AMOUNT: 1. 1-2 SHOTS, FREQUENCY: ALL, ROUTE: AM. 2. DOSE OR AMOUNT: 2-3 SHOTS, FREQUENCY: ALL, ROUTE: PM. DATES OF ABUSE: APPROXIMATELY IN 2006 TO DATE. DIAGNOSIS OR REASON FOR ABUSE: RESEARCH ON MAN KNEES? EVENT ABATED AFTER USE STOPPED OR DOSE REDUCED: 1. YES, 2. YES. EVENT REAPPEARED AFTER REINTRODUCTION: 1. YES, 2. YES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DEPUY ORTHOPEDICS KNEE REPLACEMENT JWH DEPUY UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Disability