BEUDAMED
    FDA Adverse Event Injury Summary report: N

    0112660-BARD MESH 10 X 14

    MDR report key: 370195 · Received January 4, 2002

    Report

    Report Number
    1213643-2002-00001
    Event Type
    Injury
    Date Received
    January 4, 2002
    Date of Event
    December 4, 2001
    Report Date
    January 4, 2002
    Manufacturer
    C.R. BARD, INC. (PUERTO RICO)
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    VENTRAL HERNIA REPAIR IN 1997. PATIENT HAD RECURRING VENTRAL HERNIA. MESH REMOVED IN 2001. MESH APPEARED TO HAVE TORN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 0112660-BARD MESH 10 X 14 350101100-MESH FLAT FTL C.R. BARD, INC. (PUERTO RICO) * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention