BEUDAMED
    FDA Adverse Event Other Summary report: N

    NA

    MDR report key: 199184 · Received November 24, 1998

    Report

    Report Number
    1931259-1998-00004
    Event Type
    Other
    Date Received
    November 24, 1998
    Date of Event
    October 25, 1998
    Report Date
    October 26, 1998
    Manufacturer
    CERNER CORP.
    Product Code
    MMH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    AN INCIDENT OCCURRED WHERE AN ASSOCIATE ACCESSED THE DHMC PRODUCTION (LIVE) ENVIRONMENT ON OCTOBER 25, 1998 WITHOUT AUTHORIZATION FROM PERSONNEL AT THE CLIENT SITE. THE ASSOCIATE ACCESSED THE ENVIRONMENT FOR DATABASE CONFIGURATION INQUIRY PURPOSES ONLY. DURING THE DATABASE REVIEW, THE ASSOCIATE INADVERTENTLY MODIFIED THE PATHNET HNA CLASSIC BLOOD BANK TRANSFUSION DATABASE. THE DATABASE UPDATE IMPACTED THE HISTORICAL GROUP TYPE VALIDATIONS FOR THE A POS BLOOD TYPE ONLY. THIS UPDATE IMPACTED THE COMPUTER ENTRY PROCESSES FOR THE CLIENT BUT DID NOT IMPACT PT CARE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NA * MMH CERNER CORP. NA *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other