BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BECTON DICKINSON & CO

    MDR report key: 166115 · Received April 30, 1998

    Report

    Report Number
    MW1013713
    Event Type
    Malfunction
    Date Received
    April 30, 1998
    Date of Event
    April 29, 1998
    Report Date
    April 29, 1998
    Manufacturer
    BECTON DICKINSON & CO.
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    A BECTON DICKINSON & CO 60 ML SYRINGE WAS OPENED FOR THE FIRST TIME (SEALED AROUND ALL EDGES). INSIDE SYRINGE, WRAPPED AROUND PLUNGER WERE MANY, MANY SMALL FILAMENTS OF PLASTIC-GOING IN COLOR FROM WHITE TO DIRTY GRAY. ALMOST APPEARED AS IF A SPIDER OR INSECT'S WEB HAD BEEN WOVEN IN THE PLUNGER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BECTON DICKINSON & CO 60 ML SYRINGE FMI BECTON DICKINSON & CO. * 7L646

    Patients

    Seq Age Sex Outcome Treatment
    1 *