BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD ECLIPSE

    MDR report key: 1325619 · Received December 18, 2008

    Report

    Report Number
    8041187-2008-00007
    Event Type
    Malfunction
    Date Received
    December 18, 2008
    Date of Event
    November 21, 2008
    Report Date
    December 18, 2008
    Manufacturer
    BD
    Product Code
    FMI
    PMA / PMN Number
    K010188
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REPORTER INDICATED THAT A NURSE WAS STUCK WITH A USED NEEDLE, WHILE ATTEMPTING TO CLOSE THE NEEDLE SHIED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BD ECLIPSE 3ML 25G X 1" SHIELDING HYPODERMIC SYRINGE FMI BD NA 6171976

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK