BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EPIC CPOE

    MDR report key: 6893975 · Received September 25, 2017

    Report

    Report Number
    MW5072424
    Event Type
    Injury
    Date Received
    September 25, 2017
    Date of Event
    September 14, 2017
    Report Date
    September 24, 2017
    Manufacturer
    EPIC
    Product Code
    NSX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    INNUMERABLE ORDERS ARE NOT BEING RECEIVED BY THE INTENDED RECIPIENT AND ANCILLARY SERVICE, RESULTING IN FAILURE TO COMPLETE DISEASE CRITICAL TESTS AND TREATMENTS. CARE IS DELAYED, HOSPITALIZATIONS ARE PROLONGED, DISEASES ARE WORSENING, AND PATIENTS ARE AT HIGH RISK. THE EHR DEVICE IS DEFECTIVE IN THAT THERE IS NOT ANY RECONCILIATION MECHANISM TO ALERT USERS AS TO WHAT HAS NOT BEEN DONE AS ORDERED. ONE PATIENT. ONE RECORD. ONE TEA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    670912 EPIC CPOE COMPUTERIZED PHYSICIAN ORDER ENTRY NSX EPIC
    670913 MDDS DEVICE MEDICAL DEVICE DATA SYSTEM NSX EPIC

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Hospitalization| L| O