BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CERNER

    MDR report key: 2291631 · Received October 6, 2011

    Report

    Report Number
    MW5022588
    Event Type
    Malfunction
    Date Received
    October 6, 2011
    Date of Event
    October 5, 2011
    Report Date
    October 6, 2011
    Manufacturer
    CERNER
    Product Code
    NSX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    ACCESSED THIS PATIENT'S MEDICAL RECORD IN CERNER EMR VIA CERNER POWERCHART INTERFACE AT (B)(6) HOSPITAL OF (B)(6) ON COMPUTER IP (B)(6) AT 19:12:57, YET LATER THAT SAME EVENING WHEN ACCESSING CERNER VIA POWERCHART INTERFACE AT SAME FACILITY FROM COMPUTER IP ADDRESS (B)(6) AT 20:29:59 CERNER EMR SHOWED NO EVIDENCE OF MY PRIOR ACCESS TO THIS PATIENT'S CHART AS EVIDENCED BY "RECENT" LIST ONLY SHOWING 1 PATIENT, WHICH WAS NOT THIS PATIENT. THIS IS MOST CONCERNING AS EVIDENCE OF DYSFUNCTIONAL OR NON-WORKING AUDIT TRAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CERNER POWERCHART NSX CERNER 2011-05-1-33

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR