BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SOFTBANK

    MDR report key: 274176 · Received April 11, 2000

    Report

    Report Number
    1058332-2000-00001
    Event Type
    Malfunction
    Date Received
    April 11, 2000
    Date of Event
    November 5, 1999
    Report Date
    March 31, 2000
    Manufacturer
    SCC/SOFT COMPUTER CONSULTANTS
    Product Code
    MMH
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    ATTACHMENT 1: A HOSP IDENTIFIED AN ERRONEOUS MERGE OF PT RECORDS IN SOFTBANK. TEST FROM ONE PT WERE MERGED WITH DEMOGRAPHIC INFO FROM ANOTHER AND THE PT RECORD ON WHOM THE TESTING WAS DONE WAS REMOVED FROM THE SOFTBANK DATABASE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SOFTBANK BLOOD BANK SOFTWARE MMH SCC/SOFT COMPUTER CONSULTANTS VERSIONS 19.1 AND 19.2 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Other