BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LRG TAP PRI MOD NCK 0DEG 34MM

    MDR report key: 2896152 · Received December 27, 2012

    Report

    Report Number
    9616680-2012-01512
    Event Type
    Injury
    Date Received
    December 27, 2012
    Date of Event
    December 11, 2012
    Report Date
    December 11, 2012
    Manufacturer
    STRYKER IRELAND, LTD. OSTEONICS (ORTHOPAEDICS DIVI
    Product Code
    LZO
    PMA / PMN Number
    K071082
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ADD'L INFO HAS BEEN REQUESTED AND IF RECEIVED, WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT, DOCTOR REVISED PATIENT RIGHT HIP DUE TO ALTR SERUM LEVELS CHROMIUM 2.8 COBALT 13.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LRG TAP PRI MOD NCK 0DEG 34MM IMPLANT LZO STRYKER IRELAND, LTD. OSTEONICS (ORTHOPAEDICS DIVI NA 26407701

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Required Intervention