BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SEF CENT HIP 46X28 BRN

    MDR report key: 1574645 · Received January 6, 2010

    Report

    Report Number
    1818910-2009-07922
    Event Type
    Injury
    Date Received
    January 6, 2010
    Date of Event
    December 7, 2009
    Report Date
    December 7, 2009
    Manufacturer
    DEPUY ORTHOPAEDICS, INC.
    Product Code
    KWY
    PMA / PMN Number
    K812672
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, 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

    PATIENT DISLOCATED SEVERAL TIMES AFTER PRIMARY BIPOLAR BETWEEN BIPOLAR AND NATURAL ACETABULUM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SEF CENT HIP 46X28 BRN 87KWY KWY DEPUY ORTHOPAEDICS, INC. NA D3BB41000

    Patients

    Seq Age Sex Outcome Treatment
    1 78 YR Required Intervention