BEUDAMED
    FDA Adverse Event Other Summary report: N

    BARD COMPOSIX KUGEL HERNIA PATCH

    MDR report key: 871331 · Received June 22, 2007

    Report

    Report Number
    MW5002799
    Event Type
    Other
    Date Received
    June 22, 2007
    Date of Event
    May 31, 2007
    Report Date
    June 22, 2007
    Manufacturer
    C.R. BARD INC.
    Product Code
    FTL
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WV, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    REMOVAL OF KUGEL MESH DUE TO RECURRENT VENTRAL HERNIA/INFECTED MESH. DATES OF USE: APPROX SIX MONTHS 2006 - 2007. DIAGNOSIS: VENTRAL HERNIA REPAIR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BARD COMPOSIX KUGEL HERNIA PATCH KUGEL PATCH FTL C.R. BARD INC. 43LPD513

    Patients

    Seq Age Sex Outcome Treatment
    1 YR Other