BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PHILLIPS

    MDR report key: 4121852 · Received September 22, 2014

    Report

    Report Number
    MW5038347
    Event Type
    Malfunction
    Date Received
    September 22, 2014
    Date of Event
    September 8, 2014
    Report Date
    September 22, 2014
    Manufacturer
    PHILLIPS
    Product Code
    MHX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    TELE EQUIPMENT DOWN FOR 45 MINUTES. (B)(6) CONTACTED; PTS TRIAGED APPROPRIATELY; RETURNED SPONTANEOUSLY. NO HARM TO PT. THIS DOWNTIME INCLUDED A TOTAL OF 6 PTS. NO HARM TO ANY OF THE 6 PTS OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    587538 PHILLIPS TELEMETRY MHX PHILLIPS 865139-M3150

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR