BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BECTON DICKINSON & CO.

    MDR report key: 21215 · Received July 21, 1994

    Report

    Report Number
    21215
    Event Type
    Malfunction
    Date Received
    July 21, 1994
    Date of Event
    March 6, 1994
    Report Date
    March 14, 1994
    Manufacturer
    BECTON DICKINSTON & CO
    Product Code
    KZH
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    TN, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    NURSE PUT HAND IN BOX TO TAKE OUT SYRINGE AND WAS STUCK BY NEEDLE - THROUGH WRAPPING. SYRINGE AND NEEDLE WITHOUT CAP INTACT IN WRAPPING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BECTON DICKINSON & CO. SYRINGE & PRECISION GLIDE NEEDLE 3CC 21G1 KZH BECTON DICKINSTON & CO 3K172 13

    Patients

    Seq Age Sex Outcome Treatment
    1 *