BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEWLETT PACKARD

    MDR report key: 266378 · Received February 28, 2000

    Report

    Report Number
    266378
    Event Type
    Injury
    Date Received
    February 28, 2000
    Date of Event
    January 3, 2000
    Report Date
    February 11, 2000
    Manufacturer
    AGILENT TECHNOLOGIES
    Product Code
    DRT
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    AT 0650, OBSERVED VISUALLY A 3 STAR RED ALARM READING V TACH. NO AUDIBLE ALARM OCCURRING DURING THIS EVENT. PT FOUND UNRESPONSIVE WITH VERY SHALLOW BREATHING AT 0650, PUPILS WERE UNREACTIVE. A THUMP TO THE CHEST WAS DONE WITH NO RESPONSE. PT CONTINUED TO HAVE VERY SHALLOW BREATHS. CODE WAS CALLED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEWLETT PACKARD TELEMETRY UNIT DRT AGILENT TECHNOLOGIES VIR IDA *

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Life Threatening| R