BEUDAMED
    FDA Adverse Event Injury Summary report: N

    0113680-COMPOSIX MESH 6 X 8

    MDR report key: 329494 · Received April 24, 2001

    Report

    Report Number
    1213643-2001-00021
    Event Type
    Injury
    Date Received
    April 24, 2001
    Date of Event
    January 10, 2001
    Report Date
    April 24, 2001
    Manufacturer
    C.R. BARD, INC. (PUERTO RICO)
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    DESCRIBE EVENT OR PROBLEM: BOWEL OBSTRUCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    18959 0113680-COMPOSIX MESH 6 X 8 350101104- MESH COMPOSIX FTL C.R. BARD, INC. (PUERTO RICO) * 41BIDP21

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention