Trilogy Evo EU2110X19Recalls & reported problems
Respironics, Inc. · Trilogy Evo, EU (non-BT) · Class 2
All models of Philips Trilogy Ventilator (90) · Trilogy Evo (20)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
3 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 3
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
3 FDA recall records name this device's identifier, 3 still open.
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 16, 2026.
Recalls naming this device
- Oct 7, 2024Open, Classified
Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.
Z-0291-2025 · Root cause: Device Design · Recall details · FDA record ↗
- Jul 16, 2024Open, Classified
Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.
Z-2944-2024 · Root cause: Device Design · Recall details · FDA record ↗
- Mar 19, 2024Open, Classified
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
Z-1504-2024 · Root cause: Device Design · Recall details · FDA record ↗
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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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