BEUDAMED
    FDA Adverse Event Death Summary report: N

    HEWLETT PACKARD TELEMETRY

    MDR report key: 38734 · Received September 14, 1996

    Report

    Report Number
    38734
    Event Type
    Death
    Date Received
    September 14, 1996
    Date of Event
    September 1, 1996
    Report Date
    September 9, 1996
    Manufacturer
    HEWLETT PACKARD CO.
    Product Code
    DRG
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    PT WAS ON TELEMETRY WITH ARRHYTHMIA CAPABILITIES, WHEN HE HAD AN ARREST. NO ASYSTOLE ALARM FROM SYSTEM EITHER DUE TO IMMEDIATE CLINICAL INTERVENTION BY CLINICAL STAFF OR POOR UTILIZATION OF ARRHYTHMIA COMPUTER SYSTEM. SYSTEM CHECKED BY INHOUSE BIOMED STAFF AND MFR AND FOUND TO BE FUNCTIONING CORRECTLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEWLETT PACKARD TELEMETRY TELEMETRY/ARRYTHMIA COMPUTER DRG HEWLETT PACKARD CO. M2360A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Death