BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MESH SORBA FLX OUL 08X12CM SM

    MDR report key: 2839971 · Received November 10, 2012

    Report

    Report Number
    MW5027666
    Event Type
    Injury
    Date Received
    November 10, 2012
    Manufacturer
    DAVOL- DIVISION OF BARD
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OR, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    HAD VENTRIO HERNIA MESH PUT IN ABDOMINAL WALL. TALKED TO MESH REMOVAL SPECIALIST. THE PAIN AND SWELLING IS FROM MESH REJECTION. I'M LOOKING FOR A SPECIALIST TO REMOVE IT. HORRIFIC PAIN- CONSTANT 24 HOURS A DAY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MESH SORBA FLX OUL 08X12CM SM VENTRIO MESH PATCH FTL DAVOL- DIVISION OF BARD HUW- D0708

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Other