BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CROSSLINK ANCHOR PG GLENOID 52

    MDR report key: 1962429 · Received January 7, 2011

    Report

    Report Number
    1818910-2011-00126
    Event Type
    Injury
    Date Received
    January 7, 2011
    Date of Event
    December 9, 2010
    Report Date
    December 9, 2010
    Manufacturer
    DEPUY ORTHOPAEDICS, INC.
    Product Code
    KWS
    PMA / PMN Number
    K052472
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, 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 DISLOCATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CROSSLINK ANCHOR PG GLENOID 52 87KWS KWS DEPUY ORTHOPAEDICS, INC. NA E1AKW1

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Required Intervention