BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 1011399 · Received March 10, 2008

    Report

    Report Number
    MW5005852
    Event Type
    Injury
    Date Received
    March 10, 2008
    Date of Event
    February 29, 2008
    Report Date
    March 10, 2008
    Product Code
    FWM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    BILATERAL BREAST IMPLANTS FROM 1981 RUPTURED. BILATERAL RUPTURED IMPLANTS REMOVED AND SENT TO PATHOLOGY.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 Disability