BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    B-D 10 ML SYRINGE LUER-LOK

    MDR report key: 212063 · Received March 1, 1999

    Report

    Report Number
    MW1015800
    Event Type
    Malfunction
    Date Received
    March 1, 1999
    Report Date
    February 26, 1999
    Manufacturer
    BECTON DICKINSON & CO.
    Product Code
    FMI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    ADDITIONAL INFORMATION RECEIVED FROM MANUFACTURER ON 05/25/1999: AN ADJUSTMENT WAS MADE TO A GUIDE ON THE PRINTER TO CORRECT THE PROBLEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 B-D 10 ML SYRINGE LUER-LOK SYRINGE FMI BECTON DICKINSON & CO. 309604 *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA