BEUDAMED
    FDA Adverse Event Summary report: N

    EPIC EMR

    MDR report key: 11982788 · Received June 10, 2021

    Report

    Report Number
    MW5101822
    Date Received
    June 10, 2021
    Date of Event
    June 8, 2021
    Report Date
    June 8, 2021
    Manufacturer
    EPIC SYSTEMS CORPORATION
    Product Code
    MMH
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    HOSPITAL RECENTLY CHANGED TO (B)(6). MY PATIENT HAD MRI DONE IN THIS SYSTEM. I DID NOT GET REPORT BECAUSE WE USE ANOTHER EMR. DELAY IN PHYSICIAN OVERSIGHT. COULD HAVE RESULTED IN DAMAGE TO THE PATIENT. FDA SAFETY REPORT ID# (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    874959 EPIC EMR BLOOD ESTABLISHMENT COMPUTER SOFTWARE AND ACCESSORIES MMH EPIC SYSTEMS CORPORATION IDK

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR Other