BEUDAMED
    FDA Adverse Event Injury Summary report: N

    0112650-BARD MESH 2 X 4

    MDR report key: 448821 · Received March 15, 2003

    Report

    Report Number
    1213643-2003-00014
    Event Type
    Injury
    Date Received
    March 15, 2003
    Report Date
    February 24, 2003
    Manufacturer
    C.R. BARD, INC. (PUERTO RICO)
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    PATIENT BECAME STERILE AFTER HERNIA REPAIR USING BARD MESH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 0112650-BARD MESH 2 X 4 350101100-MESH FLAT FTL C.R. BARD, INC. (PUERTO RICO) * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Disability