BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HNA MILLENNIUM RADNET

    MDR report key: 370981 · Received January 8, 2002

    Report

    Report Number
    1931259-2002-00001
    Event Type
    Malfunction
    Date Received
    January 8, 2002
    Date of Event
    September 27, 2001
    Manufacturer
    CERNER CORP.
    Product Code
    MMH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE ISSUE INVOLVES THE TEXT EDITOR CONTROL USED WITHIN THE HNAM RADNET TRANSCRIPTION APPLICATION. CERTAIN STANDARD WINDOWS KEYSTROKE COMBINATIONS AND SHORTCUTS USED IN COMBINATION WITH THE MULTIPLE SECTION LOGIC OF THE TEXT EDITOR COULD CAUSE ISSUES WITH TRUNCATION OR DELETION OF TEXT WITHIN A RADIOLOGY REPORT. ANOTHER ISSUE REPORTED WAS USERS COULD BEGIN TYPING BEFORE THE REPORT WAS FULLY LOADED, RESULTING IN MISSING TEXT. CERNER HAS NOT BEEN MADE AWARE OF ANY ADVERSE PT CARE EVENTS THAT RESULTED FROM THIS ISSUE. ALTHOUGH THE INFO IN THE REPORTS COULD BE AFFECTED, THE RISK OF ADVERSE AFFECT IS MITIGATED BY THE FACT THAT IT IS STANDARD INDUSTRY PRACTICE THAT THE RADIOLOGIST REVIEW REPORTS FOR ACCURACY BEFORE THEY ARE SIGNED AND RELEASED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HNA MILLENNIUM RADNET SOFTWARE MMH CERNER CORP. RELEASE 500 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *