BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CANON

    MDR report key: 24454687 · Received February 26, 2026

    Report

    Report Number
    2020563-2026-00001
    Event Type
    Injury
    Date Received
    February 26, 2026
    Date of Event
    February 6, 2026
    Report Date
    May 19, 2026
    Manufacturer
    CANON INC.
    Product Code
    LNH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NM, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IT WAS REPORTED THAT A PATIENT COMPLAINED OF A BURNING SENSATION ON THEIR RIGHT FOREARM AFTER THE COMPLETION OF THEIR SCAN. THE DOCTOR REPORTED OBSERVING A POSSIBLE MILD BURN/BRUISE ON THE PATIENT'S RIGHT FOREARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    398486 CANON MAGNETIC RESONANCE DIAGNOSTIC DEVICE LNH CANON INC. MEXL-1503/P3

    Patients

    Seq Age Sex Outcome Treatment
    1 76 YR Female Other