BEUDAMED
    FDA Adverse Event Death Summary report: N

    CT9000 INJECTOR

    MDR report key: 378182 · Received February 22, 2002

    Report

    Report Number
    1518293-2002-00005
    Event Type
    Death
    Date Received
    February 22, 2002
    Date of Event
    February 5, 2002
    Report Date
    February 21, 2002
    Manufacturer
    LIEBEL-FLARSHEIM
    Product Code
    DXT
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CT9000 ADV INJECTOR WAS USED ON ELDERLY PT WHO DIED ON 2002. SALES REP WAS NOTIFIED BY MEDICAL CENTER ON 2/2002. THERE IS SOME SPECULATION OF AN AIR INJECTION DUE TO AUTOPSY RESULTS SHOWING AIR IN THE PATIENTS SYSTEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CT9000 INJECTOR ANGIOGRAPHIC INJECTOR & SYRINGE DXT LIEBEL-FLARSHEIM NA *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death