BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BECTON DICKINSON & CO

    MDR report key: 336747 · Received June 8, 2001

    Report

    Report Number
    MW1022115
    Event Type
    Malfunction
    Date Received
    June 8, 2001
    Date of Event
    June 8, 2001
    Report Date
    June 8, 2001
    Manufacturer
    BECTON DICKINSON & CO
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    A BROWN "SPOTTING" FOUND ON THE INSIDE SURFACES OF ONE B-D 10ML LUER-LOK SYRINGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    26392 BECTON DICKINSON & CO 10ML LUER-LOK SYRINGE FMF BECTON DICKINSON & CO * 1082130 06

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other