BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DON'T KNOW MESH TYPE

    MDR report key: 2172061 · Received July 15, 2011

    Report

    Report Number
    MW5021418
    Event Type
    Injury
    Date Received
    July 15, 2011
    Date of Event
    January 8, 2008
    Report Date
    July 14, 2011
    Manufacturer
    UNK
    Product Code
    FTM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD MESH IMPLANTED FOR TWO INGUINAL HERNIAS. I'VE HAD CHRONIC PAIN ON THE LEFT SIDE OF GROIN SINCE THE SURGERY AND IT HAS BEEN GETTING MORE PAINFUL EVERYDAY. I'M ALSO HAVING PAIN ON THE RIGHT SIDE OF GROIN NOW. I HAVE RECEIVED MULTIPLE INJECTION TO THE MESH AREA WITH NO RELIEF. I ALSO HAVE BEEN TO PAIN MGMT AND GIVEN DIFFERENT TYPES OF DRUGS BUT NOTHING HELPS. I DON'T KNOW WHAT TYPE OF MESH WAS USED, BUT I DO KNOW THAT THERE ARE TACKS HOLDING THEM IN PLACE. THE PAIN HAS RUINED MANY THINGS IN MY LIFE, I THOUGHT I SHOULD REPORT THIS. THANKS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DON'T KNOW MESH TYPE MESH FTM UNK DONT KNOW

    Patients

    Seq Age Sex Outcome Treatment
    1 43 YR Required Intervention