BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN

    MDR report key: 1080839 · Received July 22, 2008

    Report

    Report Number
    MW5007743
    Event Type
    Injury
    Date Received
    July 22, 2008
    Date of Event
    June 12, 2008
    Report Date
    July 22, 2008
    Product Code
    FWM
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NV, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    BILATERAL REMOVE AND REPLACE BREAST IMPLANTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNKNOWN BREAST IMPLANTS FWM UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR