BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MESH

    MDR report key: 1050071 · Received May 21, 2008

    Report

    Report Number
    MW5006958
    Event Type
    Injury
    Date Received
    May 21, 2008
    Date of Event
    June 23, 2007
    Report Date
    May 21, 2008
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD A INGUINAL HERNIA REPAIR, MESH WAS USED. THE DOCTORS TELL ME THE SCAR LOOKS GOOD AND THE MESH LOOKS GOOD AFTER THE SECOND OPERATION IN 2008. I AM STILL HAVING SEVERE GROIN AND INCISION PAIN THAT GOES TO MY BELT LINE. THEY SAY THEY ARE GOING TO NOW TREAT ME FOR CHRONIC PAIN. I HAVE HAD SURGERY ON MY RIGHT SIDE AND HAVE NO PROBLEMS. MY LEFT SIDE KILLS ME. THE MESH IS SUPPOSED TO BE THE NEW STATE OF THE ART MESH. SORRY IT DOES NOT WORK AND SHOULD NOT BE USED ON ANYONE ELSE, THERE ARE TOO MANY OF US HAVING PROBLEMS. ALSO THE SURGEON SAID THE MESH COULD NOT BE REMOVED, IT WILL TO BE TOO DANGEROUS. DATES OF USE: STILL ON GOING 2007 - 2008. DIAGNOSIS OR REASON FOR USE: LEFT INGUINAL HERNIA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MESH NONE FTL

    Patients

    Seq Age Sex Outcome Treatment
    1 49 YR Hospitalization| R