BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    B-D NEEDLE

    MDR report key: 312111 · Received January 10, 2001

    Report

    Report Number
    MW1020800
    Event Type
    Malfunction
    Date Received
    January 10, 2001
    Report Date
    December 27, 2000
    Manufacturer
    BECTON DICKINSON CO.
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    BD NEEDLE 18G 1 1/2" 012708 15 NO NEEDLE IN SLEEVE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1048 B-D NEEDLE * FMI BECTON DICKINSON CO. * 012708

    Patients

    Seq Age Sex Outcome Treatment
    1 *