BEUDAMED
    FDA Adverse Event Other Summary report: N

    ETHICON INC

    MDR report key: 2744664 · Received September 11, 2012

    Report

    Report Number
    MW5026860
    Event Type
    Other
    Date Received
    September 11, 2012
    Date of Event
    November 12, 2004
    Report Date
    September 5, 2012
    Manufacturer
    JOHNSON + JOHNSON
    Product Code
    FTL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CONTINUOUS PAIN IN RIGHT GROIN AREA SINCE SURGERY FOR HERNIA REPAIR USING JOHNSON AND JOHNSON ETHICON PROLENE MESH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ETHICON INC PROLENE MESH FTL JOHNSON + JOHNSON * TDP292

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Other