BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MESH

    MDR report key: 4192817 · Received October 16, 2014

    Report

    Report Number
    MW5038699
    Event Type
    Injury
    Date Received
    October 16, 2014
    Date of Event
    February 20, 2013
    Report Date
    October 16, 2014
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AZ, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD A LUMP IN MY LOWER ABDOMEN WITH LOTS OF PAIN. I HAD IT LOOKED AT BY A DOCTOR WHO SENT ME TO HAVE AN ULTRASOUND AND MRI. HE STATED THAT I HAD A PROTRUDING HERNIA AND IT WOULD NEED TO BE REPAIRED. WE SCHEDULED SURGERY AND WHEN THE SURGERY WAS COMPLETED, HE SAID HE COULD NOT FIND THE HERNIA OR THE WHOLE IN MY STOMACH MUSCLE. HE SAID HE DID PUT IN A MESH JUST IN CASE. NOW I HAVE A CONTINUOUS PAIN AND SORENESS WHERE HE IMPLANTED THE MESH. THE AREA THERE FEELS LIKE THE MESH HAS HARDENED AND I CAN NOT BEND FORWARD WITHOUT HAVING TO LEAN TO THE SIDE. I HAVE REQUESTED MY MEDICAL RECORDS TO SEE WHAT TYPE OF MESH WAS PUT IN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    658910 MESH MESH FTL

    Patients

    Seq Age Sex Outcome Treatment
    1 43 YR