BEUDAMED
    FDA Adverse Event Summary report: N

    MCGHAN MEDICAL CORP.

    MDR report key: 277032 · Received May 4, 2000

    Report

    Report Number
    MW1018842
    Date Received
    May 4, 2000
    Date of Event
    May 3, 2000
    Report Date
    May 3, 2000
    Manufacturer
    MCGHAN MEDICAL CORP.
    Product Code
    FTR
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT HAD 510CC GEL IMPLANTS. NO PROBLEMS OR COMPLICATIONS. PT DESIRES LARGER IMPLANT. SILICONE GEL IMPLANTS REMOVED INTACT WITHOUT PROBLEMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MCGHAN MEDICAL CORP. SILICONE MAMMARY IMPLANTS FTR MCGHAN MEDICAL CORP. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 29 YR