BEUDAMED
    FDA Adverse Event Injury Summary report: N

    WRIGHT CONSERVE PLUS HIP IMPLANT

    MDR report key: 2652199 · Received July 8, 2012

    Report

    Report Number
    MW5026104
    Event Type
    Injury
    Date Received
    July 8, 2012
    Date of Event
    May 1, 2012
    Report Date
    July 8, 2012
    Manufacturer
    WRIGHT
    Product Code
    KWA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    POPPING OR CLICKING OF WRIGHT CONSERVE PLUS HIP IMPLANT DEVICE THAT WAS INSERTED IN (B)(6) 2007. I HAVE BEEN FEELING FINE - NO PROBLEMS UNTIL THE RIGHT HIP STARTED CLICKING OR POPPING. THE PROBLEM HAS BEEN INCREASING OVER THE LAST 2 WEEKS. I AM UNABLE TO EXERCISE AND DO MUCH WALKING. I AM AFRAID OF CAUSING MORE METAL IONS TO BE RELEASED IN MY BODY AND I DON'T KNOW THE LONG TERM EFFECTS. I AM BECOMING INCREASINGLY UNCOMFORTABLE AND MY DR HAS SAID THAT I MAY NEED A REVISION. I WANTED TO DO PHYSICAL THERAPY BUT I HAVE DECIDED NOT TO. I AM AFRAID OF CAUSING MORE DAMAGE TO THE HIP AND I DON'T THINK IT WILL DO ANY GOOD. I AM VERY DEPRESSED ABOUT HAVING TO UNDERGO ANOTHER HIP SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 WRIGHT CONSERVE PLUS HIP IMPLANT HIP IMPLANT DEVICE KWA WRIGHT

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR Other| R| S