BEUDAMED
    FDA Adverse Event Death Summary report: N

    MRIDIUM MRI INFUSION PUMP

    MDR report key: 24388942 · Received February 19, 2026

    Report

    Report Number
    MW5184080
    Event Type
    Death
    Date Received
    February 19, 2026
    Date of Event
    January 21, 2026
    Report Date
    February 13, 2026
    Manufacturer
    IRADIMED CORPORATION
    Product Code
    FRN
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AZ, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    ON (B)(6) 2026, PATIENT SUFFERED A CARDIAC EVENT DUE TO MEDICATION BEING DISCONNECTED FROM AN MRI PUMP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    454059 MRIDIUM MRI INFUSION PUMP PUMP, INFUSION FRN IRADIMED CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Male Life Threatening| D