BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CT 9000 INJECTOR

    MDR report key: 188396 · Received September 21, 1998

    Report

    Report Number
    1518293-1998-00020
    Event Type
    Injury
    Date Received
    September 21, 1998
    Date of Event
    October 24, 1997
    Report Date
    September 21, 1998
    Manufacturer
    LIEBEL-FLARSHEIM CO.
    Product Code
    DXT
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    AIR INJECTION INTO PT'S CHEST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CT 9000 INJECTOR ANGIOGRAPHIC CT INJECTOR DXT LIEBEL-FLARSHEIM CO. NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Life Threatening