BEUDAMED
    FDA Adverse Event Other Summary report: N

    CODEMASTER XL

    MDR report key: 307296 · Received November 29, 2000

    Report

    Report Number
    1218950-2000-00227
    Event Type
    Other
    Date Received
    November 29, 2000
    Report Date
    October 24, 2000
    Manufacturer
    AGILENT TECHNOLOGIES, INC
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    THE FOLLOWING PROBLEM WAS REPORTED TO AGILENT TECHNOLOGIES: IN 2000, WHEN THE PACER MODE WAS TURNED ON, THE STAFF SAW DASHED LINES ON THE ECG SCREEN. THE PT WAS SWITCHED TO BACK-UP EQUIPMENT AND THERE WAS NO ADVERSE OUTCOME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CODEMASTER XL DEFIB/MON/REC LDD AGILENT TECHNOLOGIES, INC M1722A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA