BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PHILIPS RESPIRONICS TRILOGY EVO VENTILATOR

    MDR report key: 25047054 · Received April 30, 2026

    Report

    Report Number
    MW5187505
    Event Type
    Injury
    Date Received
    April 30, 2026
    Date of Event
    April 3, 2026
    Report Date
    April 27, 2026
    Manufacturer
    RESPIRONICS, INC./PHILIPS MEDICAL SYSTEMS INTERNATIONAL BV
    Product Code
    NOU
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    THE PATIENT'S VENTILATOR WAS UPDATED WITH A NEW SOFTWARE. THE PATIENT WAS USING THE VENTILATOR AFTER THE SOFTWARE UPDATE AND THE VENT MALFUNCTIONED/STOPPING WORKING. THE PATIENT'S VENT WAS SWITCHED OUT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    373508 PHILIPS RESPIRONICS TRILOGY EVO VENTILATOR CONTINUOUS, VENTILATOR, HOME USE NOU RESPIRONICS, INC./PHILIPS MEDICAL SYSTEMS INTERNATIONAL BV

    Patients

    Seq Age Sex Outcome Treatment
    1