BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SOFTID.NET

    MDR report key: 1470917 · Received August 21, 2009

    Report

    Report Number
    1058332-2009-00001
    Event Type
    Malfunction
    Date Received
    August 21, 2009
    Report Date
    May 29, 2009
    Manufacturer
    SCC SOFT COMPUTER
    Product Code
    JQP
    Removal / Correction Number
    1058332-08/20/2009-003-C
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    INSPECTED SOURCE CODE OF PROGRAM. THE 'ALLOW TO CANCEL' CAN BE DESELECTED FROM THE ADMINISTRATIVE CONSOLE (FOR EVERY ROLE) TO DISALLOW THE USERS FROM CANCELLING ANY ORDERS FROM THE (B) (4) APPLICATION FOR RELEASE LOWER THAN (B) (4). THE USER MAY CANCEL THE ORDER USING SOFTLAB ORDER ENTRY.

    Description of Event or Problem · 1

    WHEN A PATIENT WAS CANCELLED OR RE-SCHEDULED FROM THE CONTEXT MENU, THE PATIENT WAS SELECTED BASED ON THE PATIENT INDEX ON THE LIST. AN INCORRECT PATIENT WAS BEING PULLED FOR CANCELLATION OR RE-SCHEDULING, BECAUSE THE PATIENT INDEX WAS CHANGED WITH AUTOMATIC UPDATE. THIS CAUSED A DIFFERENT PATIENT ORDER TO BE CANCELLED WHILE COMMENTS WERE BEING ADDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SOFTID.NET JQP SCC SOFT COMPUTER

    Patients

    Seq Age Sex Outcome Treatment
    1