BEUDAMED
    FDA Adverse Event Injury Summary report: N

    0113680-COMPOSIX MESH 6 X 8

    MDR report key: 303202 · Received October 30, 2000

    Report

    Report Number
    1213643-2000-00060
    Event Type
    Injury
    Date Received
    October 30, 2000
    Date of Event
    June 1, 2000
    Report Date
    October 30, 2000
    Manufacturer
    C.R. BARD, INC. (PUERTO RICO)
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    PT INFECTION. MESH PLACED APPROX 2000. PT DEVELOPED INFECTION SEVERAL DAYS POST-OP. MESH REMOVED APPROX 2 MONTHS POST-OP. PT RECOVERED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 0113680-COMPOSIX MESH 6 X 8 350101104-MESH COMPOSIX FTL C.R. BARD, INC. (PUERTO RICO) * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *