BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD

    MDR report key: 1091163 · Received July 31, 2008

    Report

    Report Number
    MW5007869
    Event Type
    Malfunction
    Date Received
    July 31, 2008
    Date of Event
    July 31, 2008
    Report Date
    July 31, 2008
    Manufacturer
    BECTON DICKINSON & CO.
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    UNOPENED BD 18G1-1/2 NEEDLE MISSING A PIECE OF THE CAP, EXPOSING THE SHARP END OF THE NEEDLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD 18G 1-1/2 PRECISIONGLIDE NEEDLE FMI BECTON DICKINSON & CO. 305196 7341778

    Patients

    Seq Age Sex Outcome Treatment
    1