BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MAMMARY PROSTHESIS

    MDR report key: 158084 · Received March 19, 1998

    Report

    Report Number
    6000080-1998-00718
    Event Type
    Injury
    Date Received
    March 19, 1998
    Date of Event
    January 1, 1979
    Report Date
    March 13, 1998
    Manufacturer
    AMERICAN HEYER-SCHULTE
    Product Code
    FTR
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED VIA MEDWATCH 1012800 THAT THE CONSUMER EXPERIENCED VARIOUS ILLNESSES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAMMARY PROSTHESIS Implant BREAST IMPLANT FTR AMERICAN HEYER-SCHULTE UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other