BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HERNIA MESH

    MDR report key: 2202210 · Received August 7, 2011

    Report

    Report Number
    MW5021680
    Event Type
    Injury
    Date Received
    August 7, 2011
    Date of Event
    August 31, 2010
    Report Date
    August 7, 2011
    Manufacturer
    DAVOL BARD
    Product Code
    FTL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAVE HAD 4 HERNIA SURGERIES IN THE PAST 2 YEARS, ALL ON THE SAME HERNIA. NOW I HAVE PAIN DISCOMFORT ALL THE TIME.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR Hospitalization