BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESPIRONICS ESPIRIT

    MDR report key: 4231947 · Received October 31, 2014

    Report

    Report Number
    MW5038977
    Event Type
    Malfunction
    Date Received
    October 31, 2014
    Date of Event
    October 29, 2014
    Report Date
    October 31, 2014
    Manufacturer
    PHILIPS
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    VENT POWERED OFF WHILE IN USE AND EXTERNAL BATTERY LIGHT CAME ON.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    698480 RESPIRONICS ESPIRIT VENTILATOR CBK PHILIPS V1000

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR