BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BD

    MDR report key: 3070438 · Received April 16, 2013

    Report

    Report Number
    MW5029844
    Event Type
    Malfunction
    Date Received
    April 16, 2013
    Date of Event
    April 12, 2013
    Report Date
    April 16, 2013
    Manufacturer
    BD
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IN, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    PLASTIC SYRINGE APPEARS TO HAVE BROWN PARTICLES EMBEDDED IN THE PLASTIC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    164007 BD SYRINGE FMF BD N 34

    Patients

    Seq Age Sex Outcome Treatment
    1