Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator devi
Pending LLM rewrite. Source: FDA_DEVICE Z-1647-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.
The recalled product
- Product
- Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
- Manufacturer
- Philips Respironics, Inc.
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- All Model No.
- All UDI
- All Serial No.
Distribution
Distributed nationwide across the United States.
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