BEUDAMED
    FDA Adverse Event Other Summary report: N

    MEDRAD ANGIOGRAPHIC INJECTOR

    MDR report key: 107634 · Received July 23, 1997

    Report

    Report Number
    2520313-1997-00029
    Event Type
    Other
    Date Received
    July 23, 1997
    Date of Event
    June 23, 1997
    Report Date
    July 22, 1997
    Manufacturer
    MEDRAD, INC.
    Product Code
    DXT
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    HOSP PERSONNEL REPORTED THAT 68 ML OF CONTRAST WAS DELIVERED WHEN 34 ML WAS DESIRED. NO INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDRAD ANGIOGRAPHIC INJECTOR ANGIOGRAPHIC INJECTOR DXT MEDRAD, INC. MKV NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other