BEUDAMED
    FDA Adverse Event Other Summary report: N

    MEDRAD ANGIOGRAPHIC INJECTOR

    MDR report key: 217718 · Received April 5, 1999

    Report

    Report Number
    2520313-1999-00018
    Event Type
    Other
    Date Received
    April 5, 1999
    Date of Event
    March 19, 1999
    Report Date
    April 1, 1999
    Manufacturer
    MEDRAD, INC.
    Product Code
    DXT
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    WHEN THE HOSPITAL WENT TO MOVE THE INJECTOR, ONE OF THE TECHNOLOGIES GRABBED HOLD OF THE HEAD; NOT REALIZING THE WEIGHT OF IT, SHE DROPPED IT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other