Trilogy Evo FX2110X15BRecalls & reported problems
Respironics, Inc. · Trilogy Evo, International · Class 2
All models of Philips Trilogy Ventilator (90) · Trilogy Evo (20)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00606959061026), received between Sep 4, 2024 and Sep 4, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 4, 2024Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
A VENTILATOR WAS RETURNED TO A THIRD PARTY SERVICE CENTER FOR ROUTINE PREVENTIVE MAINTENANCE. THERE WAS NO ALLEGATION OF DEVICE MALFUNCTION. THE DEVICE WAS NOT IN PATIENT USE. DURING THE EVALUATION OF THE DEVICE AT THE THIRD PARTY SERVICE CENTER, THE DEVICE FAILED A STEP DURING TESTING. THE DEVICE'S ACTIVE EXHALATION CONTROL MODULE MAIN BOARD, AND 3 WAY SOLENOID VALVE WERE REPLACED TO ADDRESS THE ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20141002 ↗
Other Continuous, ventilator, home use devices
- Astral 150Resmed Pty Ltd · Continuous, Ventilator, Home Use1 recall17 deaths2,361 reports
- Trilogy EV300, USA DS2200X11BRespironics, Inc. · Continuous, ventilator, home use5 recalls2,071 reports
- Trilogy 00Respironics, Inc. · CONTINUOUS, VENTILATOR, HOME USE15 deaths2,059 reports
- Trilogy Evo, Japan JP2110X16BRespironics, Inc. · Continuous, ventilator, home use5 recalls27 deaths1,112 reports
- Astral 100Resmed Pty Ltd · Continuous, Ventilator, Home Use9 deaths865 reports
- Trilogy Trilogy Evo Ventilator, IntlRespironics, Inc. · CONTINUOUS, VENTILATOR, HOME USE4 recalls3 deaths648 reports
- Life2000 MS-01-0118Welch Allyn, Inc. · Continuous, ventilator, home use10 recalls2 reports
- Trilogy Evo GB2110X15BRespironics, Inc. · Continuous, ventilator, home use5 recalls1 death141 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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