BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ASR UNI FEMORAL IMPL SIZE 51

    MDR report key: 2232169 · Received September 2, 2011

    Report

    Report Number
    1818910-2011-17057
    Event Type
    Injury
    Date Received
    September 2, 2011
    Report Date
    August 5, 2011
    Manufacturer
    DEPUY INTERNATIONAL
    Product Code
    KWA
    PMA / PMN Number
    K040627
    Removal / Correction Number
    Z-1749/1816-2011
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Additional Manufacturer Narrative · 1

    THE ASR PLATFORM WAS VOLUNTARILY RECALLED FROM THE MARKET IN (B)(4) 2010, AND THE ASR PRODUCT CODES ARE NOW CONSIDERED INACTIVE. FURTHER INVESTIGATION OF THIS INDIVIDUAL INCIDENT WILL NOT BE UNDERTAKEN, AS THERE IS AN ONGOING INVESTIGATION REGARDING THE ROOT CAUSE(S) AND/OR CORRECTIVE ACTIONS. (B)(4). DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.

    Description of Event or Problem · 1

    LITIGATION PAPERS ALLEGE THE PATIENT IS EXPERIENCING SIGNIFICANT AND PERMANENT PERSONAL INJURY INCLUDING, BUT NOT LIMITED TO RELEASE OF METAL AND METAL IONS INTO HIS THE PATIENT SUSTAINED SIGNIFICANT ECONOMIC DAMAGE, INTERFERENCE WITH DAILY LIVING ACTIVITIES AND INTERFERENCE WITH HIS ABILITY TO PERFORM OTHER ECONOMICALLY PRODUCTIVE ENTERPRISES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASR UNI FEMORAL IMPL SIZE 51 FEMORAL HEAD HIP IMPLANT KWA DEPUY INTERNATIONAL 2372510

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention