BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LCS CRUC M/B PAT REPLAC GVF LG

    MDR report key: 1581430 · Received January 15, 2010

    Report

    Report Number
    1818910-2009-08041
    Event Type
    Injury
    Date Received
    January 15, 2010
    Date of Event
    December 16, 2009
    Report Date
    December 16, 2009
    Manufacturer
    DEPUY ORTHOPAEDICS, INC.
    Product Code
    NJL
    PMA / PMN Number
    P8300055
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, 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 WAS REVISED TO ADDRESS INFECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LCS CRUC M/B PAT REPLAC GVF LG 87NJL NJL DEPUY ORTHOPAEDICS, INC. NA 2410367

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Required Intervention