BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BECTON DICKINSON & CO

    MDR report key: 200544 · Received November 20, 1998

    Report

    Report Number
    MW4002388
    Event Type
    Malfunction
    Date Received
    November 20, 1998
    Date of Event
    November 19, 1998
    Report Date
    November 20, 1998
    Manufacturer
    BECTON DICKINSON & CO.
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    4-B-D 3CC SYRINGES WITH 21 GAUGE 1 1/2 INCH NEEDLES HAD NO MARKINGS FOR MEASUREMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BECTON DICKINSON & CO SYRINGE 3CC & 21 G 1 1/2 IN NEEDLE FMI BECTON DICKINSON & CO. 309577 8G223 13
    2 BECTON DICKINSON & COMPANY SYRINGE 3CC & 21G 1 1/2IN NEEDLE FMI BECTON DICKINSON & CO. 309577 8G223 10
    3 BECTON DICKINSON & COMPANY SYRINGE 3CC & 21G 1 1/2IN NEEDLE FMI BECTON DICKINSON & CO. 309577 8G223 16
    4 BECTON DICKINSON & COMPANY SYRINGE 3CC & 21G 1 1/2IN NEEDLE FMI BECTON DICKINSON & CO. 309577 8G223 14

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other