BEUDAMED
    FDA Adverse Event No answer provided Summary report: N

    CATHETER, INTRAVASCULAR, DIAGNOSTIC

    MDR report key: 14564552 · Received June 1, 2022

    Report

    Report Number
    14564552
    Event Type
    No answer provided
    Date Received
    June 1, 2022
    Date of Event
    April 16, 2022
    Report Date
    April 16, 2022
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    DQO
    Report Source
    User Facility report
    Reporter Location
    PA
    Reporter Occupation
    RISK MANAGER
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    MID 40¿S WOMAN WITH LEFT VERTEBRAL ARTERY DISSECTION AND BASILAR OCCLUSION. PATIENT PRESENTED FOR CEREBRAL ANGIOGRAPHY AND MECHANICAL THROMBECTOMY. MRI ON THE FOLLOWING DAY IDENTIFIED A FOCAL AREA OF SUSCEPTIBILITY IN THE RIGHT OCCIPITAL LOBE. MRI CONFIRMED ARTIFACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1460721 CATHETER, INTRAVASCULAR, DIAGNOSTIC DQO MEDTRONIC, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown