BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK

    MDR report key: 2585103 · Received May 17, 2012

    Report

    Report Number
    MW5025461
    Event Type
    Injury
    Date Received
    May 17, 2012
    Date of Event
    October 10, 2011
    Report Date
    May 17, 2012
    Manufacturer
    NA
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD TWO HERNIAS REMOVED, AND IMPLANTED WITH MESH. I HAVE SEVERE PAIN THAT MAKES ME CRY AND IT HURTS FOR ME TO WALK STRAIGHT UP. I HAVE DIFFICULT URINATION, IT FEELS LIKE MY STOMACH IS ABOUT TO FALL OUT. I HAVE BEEN BACK TO THE SURGEON MANY TIMES. HE SUGGESTED THAT I SEE A GASTROENTEROLOGY, I DID, NOTHING IS WRONG THERE. PLEASE HELP ME I'M IN GREAT PAIN. REASON FOR USE: HERNIA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK MESH FTL NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 36 YR Other