BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DURALOC CONST LINER 58/70X32

    MDR report key: 1120736 · Received August 14, 2008

    Report

    Report Number
    1818910-2008-03634
    Event Type
    Injury
    Date Received
    August 14, 2008
    Date of Event
    July 15, 2008
    Report Date
    July 15, 2008
    Manufacturer
    DEPUY ORTHOPAEDICS, INC.
    Product Code
    JDI
    PMA / PMN Number
    P960054/S02
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

    Description of Event or Problem · 1

    PT REVISED FOR CHRONIC DISLOCATION. UNK MANUFACTURER OF HEAD LEFT IN PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DURALOC CONST LINER 58/70X32 87JDI JDI DEPUY ORTHOPAEDICS, INC. NA X5EGJ1000

    Patients

    Seq Age Sex Outcome Treatment
    1 76 YR Required Intervention