BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD PRECISION GLIDE NEEDLE / INJECTION

    MDR report key: 8362957 · Received February 21, 2019

    Report

    Report Number
    MW5084230
    Event Type
    Malfunction
    Date Received
    February 21, 2019
    Date of Event
    February 18, 2019
    Report Date
    February 18, 2019
    Manufacturer
    BECTON, DICKINSON AND COMPANY
    Product Code
    FMI
    UDI-DI
    00382903051298
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    BECTON, DICKINSON AND COMPANY, BD PRECISION GLIDE NEEDLE, 21G X 2 (0.8MM X 50MM) INJECTION NEEDLE NOT INCLUDED IN SEALED, STERILE PACKAGING. ONLY THE CAP WAS IN THE PACKAGING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    150513 BD PRECISION GLIDE NEEDLE / INJECTION NEEDLE, HYPODERMIC, SINGLE LUMEN FMI BECTON, DICKINSON AND COMPANY 305129 8250832 00382903051298

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR