BEUDAMED
    FDA Adverse Event Summary report: N

    BECKER EXPANDER/MAMMARY PROSTHESIS

    MDR report key: 13366 · Received May 18, 1994

    Report

    Report Number
    MW1002087
    Date Received
    May 18, 1994
    Date of Event
    June 17, 1991
    Report Date
    May 6, 1994
    Manufacturer
    MENTOR CORP.
    Product Code
    FTR
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    RPTR COMPLAINS OF PAIN IN KNEES, HIPS, SHOULDERS, HANDS, FINGERS AND LEFT CHEST, BREAST HARDNESS, PAINFUL BREASTS, ITCHING, FATIGUE, SWELLING OF HANDS AND FEET, HAIR LOSS, AND INFECTIONS. (SEE ALSO 1002085 AND 1002086.)

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BECKER EXPANDER/MAMMARY PROSTHESIS Implant FTR MENTOR CORP. 58410

    Patients

    Seq Age Sex Outcome Treatment
    1 *