BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HERNIA REPAIR MESH

    MDR report key: 1052150 · Received May 26, 2008

    Report

    Report Number
    MW5007029
    Event Type
    Injury
    Date Received
    May 26, 2008
    Date of Event
    February 8, 2007
    Report Date
    May 26, 2008
    Product Code
    FTL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    HAD AN INGUINAL HERNIA REPAIR, HAVE HAD SEVERE GROIN PAIN SINCE SURGERY WAS DONE, HAVE BEEN TO MULTIPLE DOCTORS, A SURGEON JUST TOLD ME THAT I HAVE AN ENTRAPPED NERVE IN THE MESH THAT WAS USED FOR THE SURGERY. I AM IN SEVERE PAIN. I DO NOT HAVE A LIFE ANYMORE, CANNOT URINATE PROPERLY, CANNOT MAKE LOVE TO MY WIFE -HURTS TOO BAD-, CANNOT PLAY WITH MY KIDS - RUNNING, JUMPING ETC-, WALK FOR PERIODS OF TIME, LAY ON MY LEFT SIDE. I HAVE FLUID IN MY LEFT TESTICLE AND MY SCROTUM AREA IS SWOLLEN AND SENSITIVE TO TOUCH. I NEED MORE INFO ON THIS. I AM CONTACTING THE DR AND THE HOSP WHERE I HAD SURGERY TO GET THE RECORDS, SO I CAN GET THE NAME OF THE MESH THAT WAS USED ON ME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HERNIA REPAIR MESH FTL

    Patients

    Seq Age Sex Outcome Treatment
    1 39 YR Other NOT SURE