BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AGILENT INFO CENTER

    MDR report key: 445717 · Received March 3, 2003

    Report

    Report Number
    1218950-2003-00029
    Event Type
    Injury
    Date Received
    March 3, 2003
    Date of Event
    February 2, 2003
    Report Date
    February 3, 2003
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    DRT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE CENTRAL STATION DID NOT ALARM FOR ASYSTOLE OR BRADYCARDIA. THE PT HAD A SEIZURE AND WAS ADMITTED TO ICU.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AGILENT INFO CENTER CENTRAL STATION MONITOR DRT AGILENT TECHNOLOGIES, INC. M3150A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Life Threatening