BEUDAMED
    FDA Adverse Event Injury Summary report: N

    0112760-BARD MESH MED PERFIX

    MDR report key: 314622 · Received January 30, 2001

    Report

    Report Number
    1213643-2001-00006
    Event Type
    Injury
    Date Received
    January 30, 2001
    Date of Event
    October 19, 2000
    Report Date
    January 27, 2001
    Manufacturer
    C.R. BARD, INC. (PUERTO RICO)
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT INFECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    3666 0112760-BARD MESH MED PERFIX 350102102-MESH PLUGS FTL C.R. BARD, INC. (PUERTO RICO) * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Life Threatening