BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ASR ACETABULAR CUPS 50

    MDR report key: 3183249 · Received June 21, 2013

    Report

    Report Number
    1818910-2013-19567
    Event Type
    Injury
    Date Received
    June 21, 2013
    Date of Event
    April 2, 2015
    Report Date
    April 2, 2015
    Manufacturer
    DEPUY INTL., LTD. - 8010379
    Product Code
    KWA
    PMA / PMN Number
    PK040627
    Removal / Correction Number
    Z-1749/1816-2011
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Additional Manufacturer Narrative · 1

    THE ASR PLATFORM WAS VOLUNTARILY RECALLED FROM THE MARKET IN AUGUST 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.

    Additional Manufacturer Narrative · 1

    DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED

    Additional Manufacturer Narrative · 1

    THERE IS NO NEW INFORMATION THAT WOULD CHANGE THE OUTCOME OF THE INVESTIGATION. THE COMPLAINT IS CONSIDERED CLOSED.

    Description of Event or Problem · 1

    LITIGATION PAPERS RECEIVED ALLEGING THAT THE PATIENT SUFFERS FROM PAIN, ACHING IN JOINT, AND A POPPING SOUND WHEN SHE WALKS. ALSO ALLEGED IS ELEVATED METAL IONS.

    Description of Event or Problem · 1

    ASR REVISION.ASR XL - RIGHT HIP.REASON FOR REVISION: PAIN, NOISE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    283958 ASR ACETABULAR CUPS 50 TOTAL HIP REPLACEMENT KWA DEPUY INTL., LTD. - 8010379 2833729

    Patients

    Seq Age Sex Outcome Treatment
    1 70 YR Other| R