BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRIOLOGY EVO

    MDR report key: 25095270 · Received May 6, 2026

    Report

    Report Number
    MW5187776
    Event Type
    Injury
    Date Received
    May 6, 2026
    Date of Event
    April 30, 2026
    Report Date
    May 1, 2026
    Manufacturer
    RESPIRONICS INC./PHILIPS MEDICAL SYSTEMS INTERNATIONAL BV
    Product Code
    CBK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    VENTILATOR WAS BLOWING AIR LOUDLY. PATIENT WAS PLACED ON BACK UP VENTILATOR AND PRIMARY DISPLAY MESSAGE SHOWED VENTILATOR INOPERABLE AND THEN POWERED DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    344424 TRIOLOGY EVO VENTILATOR, CONTINUOUS, FACILITY USE CBK RESPIRONICS INC./PHILIPS MEDICAL SYSTEMS INTERNATIONAL BV

    Patients

    Seq Age Sex Outcome Treatment
    1