BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SOFTLAB

    MDR report key: 2167972 · Received June 16, 2011

    Report

    Report Number
    1058332-2011-00003
    Event Type
    Malfunction
    Date Received
    June 16, 2011
    Report Date
    June 14, 2011
    Manufacturer
    SCC SOFT COMPUTER
    Product Code
    JQP
    Removal / Correction Number
    1058332-06/02/2009-002-C
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE CLIENT REPORTED THE PRODUCT MALFUNCTION ON SOFTLAB 4.0.3.13.2 AFFECTED VERSIONS INCLUDE: 4.0.1.0-4.0.1.16, 4.0.2.0-4.0.2.10, 4.0.3.0-4.03.13, 4.0.4.0-4.0.4.5. METHOD: INSPECTED SOURCE CODE OF PROGRAM.

    Description of Event or Problem · 1

    CLIENT WAS USING PATIENT MAINTENANCE TO PERFORM MOVES OF STAYS OPERATION WHICH SUBSEQUENTLY SENT THE WRONG BILLING NUMBER DURING AN ADT UPDATE TO SOFTWEB, SOFTPATH AND SOFTMEDIA. THE INCORRECT BILLING NUMBER TRANSMITTED VIA INTERNAL ADT TO SOFTWEB, SOFTPATH AND SOFTMEDIA WERE THEN APPLIED TO A DIFFERENT PATIENT RECORDS. BILLING NUMBERS IN SOFTLAB WERE CORRECT. EXTERNAL ADT TRANSACTIONS WERE NOT AFFECTED. NO ADVERSE PATIENT EVENT IS ASSOCIATED WITH THIS ISSUE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1