BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ZYMED (AGILENT TECHNOLOGIES)

    MDR report key: 315036 · Received February 7, 2001

    Report

    Report Number
    315036
    Event Type
    Injury
    Date Received
    February 7, 2001
    Date of Event
    January 29, 2001
    Report Date
    February 6, 2001
    Manufacturer
    ZYMED
    Product Code
    DRG
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    PT WENT INTO V-FIB AND UNIT DID NOT ALARM. MONITOR TECH OBSERVED PT WAS IN V-FIB AND ALARM DIDN'T SOUND. PT WAS FOUND TO BE IN CARDIAC ARREST. PT WAS SUCCESSFULLY RESUSCITATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    4511 ZYMED (AGILENT TECHNOLOGIES) MONITORING SYSTEM/TELEMETRY DRG ZYMED HP VIETRA VL TRANSMITTER #2 NO SERIAL #

    Patients

    Seq Age Sex Outcome Treatment
    1 76 YR Hospitalization| R