BEUDAMED
    FDA Adverse Event Other Summary report: N

    BECTON DICKSON

    MDR report key: 475506 · Received July 30, 2003

    Report

    Report Number
    MW1029145
    Event Type
    Other
    Date Received
    July 30, 2003
    Report Date
    July 30, 2003
    Manufacturer
    *
    Product Code
    FBK
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    WHEN USING BECTON DICKSON BLUNT PLASTIC CANNULAS TO ACCESS A VIAL REPORTER HAS SOMETIMES NOTICED A SMALL PIECE OF THE RUBBER STOPPER FROM THE VIAL IN THE SYRINGE AFTER ASPIRATING THE CONTENTS OF THE VIAL. REPORTER ALWAYS DISCARDS THE SYRINGE BUT REPORTER HAS CONCERNS THAT THIS PARTICLE MIGHT BE INJECTED INTO A PT. EITHER IM OR IV. REPORTER WOULD LIKE TO KNOW IF OTHERS HAVE REPORTED THIS PROBLEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BECTON DICKSON BLUNT PLASTIC CANNULA FBK * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other