BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BECTON DICKINSON AND CO.

    MDR report key: 321035 · Received March 13, 2001

    Report

    Report Number
    MW1021348
    Event Type
    Malfunction
    Date Received
    March 13, 2001
    Date of Event
    January 22, 2001
    Report Date
    March 13, 2001
    Manufacturer
    BECTON DICKINSON AND CO.
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SC, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    THE NEW B&D 3 CC SYRINGES POP OFF WHEN INJECTING THE PT WITH RADIOPHARMACEUTICAL DURING PROCEDURE. SPLASH ON FLOOR, PERSONNEL, AND TREADMILL. ROOM HAD TO BE CLOSED FOR 24 HRS FOR DECONTAMINATION. PT OK. COMPLAINTS OF FROM OTHER HEALTH CARE PROVIDERS IN THE FACILITY CONCERNING THIS SYRINGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    11046 BECTON DICKINSON AND CO. BLUNT TIP SYRINGES FMF BECTON DICKINSON AND CO. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Other