BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    V SERIES MONITOR

    MDR report key: 3091786 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00290
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    February 8, 2013
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    MHX
    PMA / PMN Number
    102004
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER WAS ASSISTED IN MODIFYING SYSTEM SETTINGS, WHICH RESOLVED THE ISSUE.

    Description of Event or Problem · 1

    CUSTOMER REPORTED V SERIES MONITOR WAS FALSELY READING V TACH. THIS OCCURED AFTER A PACEMAKER WAS INSERTED, POST A PATIENT CODE. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    188121 V SERIES MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1