BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CT 9000 INJECTOR

    MDR report key: 189274 · Received September 25, 1998

    Report

    Report Number
    1518293-1998-00021
    Event Type
    Injury
    Date Received
    September 25, 1998
    Date of Event
    August 25, 1998
    Report Date
    September 25, 1998
    Manufacturer
    LIEBEL-FLARSHEIM CO.
    Product Code
    DXT
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    WHEN INJECTING PT, INFILTRATION OF 60 - 75 CC INTO PT'S ARM.

    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 Other