BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    B-D

    MDR report key: 439219 · Received January 7, 2003

    Report

    Report Number
    MW4003442
    Event Type
    Malfunction
    Date Received
    January 7, 2003
    Date of Event
    December 20, 2002
    Manufacturer
    B-D
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CT, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    1ML 25G 5/8 TUBERCULIN SYRINGE MADE BY B-D WAS PACKAGED WITH NO CAP ON NEEDLE. WHO DISCOVERED THE ERROR? PHARMACY TECHNICIAN. WHEN AND HOW WAS ERROR DISCOVERED? IN IV ROOM PREPARING IV'S. WHERE DID THE ERROR OCCUR? HOSPITAL PHARMACY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 B-D * FMF B-D * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *