BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD STERILE NEEDLES

    MDR report key: 1514225 · Received October 20, 2009

    Report

    Report Number
    MW5013115
    Event Type
    Malfunction
    Date Received
    October 20, 2009
    Report Date
    October 8, 2009
    Manufacturer
    B-D
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WI, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    PRODUCT PROBLEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD STERILE NEEDLES BD STERILE NEEDLES, 25 G X 8MM FMI B-D 7061169
    2 B-D STERILE NEEDLES BD STERILE NEEDLES, 25 G X 8MM FMI B-D 7061169
    3 B-D STERILE NEEDLES BD STERILE NEEDLES, 25G X 8MM FMI B-D 7061169
    4 B-D STERILE NEEDLES BD STERILE NEEDLES 25G X 8MM FMI B-D 7061169
    5 BD ULTRAFINE PEN NEEDLE BOX BD ULTRAFINE PEN NEEDLE BOX, 29G 12.7MM FMI B-D

    Patients

    Seq Age Sex Outcome Treatment
    1