BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SURGICAL MESH

    MDR report key: 3944467 · Received July 14, 2014

    Report

    Report Number
    MW5037272
    Event Type
    Injury
    Date Received
    July 14, 2014
    Date of Event
    July 3, 2012
    Report Date
    July 11, 2014
    Manufacturer
    UNK
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    SURGERY TO REPAIR ABDOMINAL LLQ HERNIA POST C-SECTION ON (B)(6) 2012. THREE MONTHS POST SURGERY PAIN WORSENED TO THE DEGREE TODAY THAT I AM SEVERELY LIMITED IN PHYSICAL ACTIVITY AND BECOMING DEPRESSED FROM THE DAILY PAIN AND PHYSICAL DISABILITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    409935 SURGICAL MESH MESH FTL UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 42 YR Disability