Official recall record
Trilogy Evo and Trilogy Ev300
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-10-02
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Philips Respironics has become aware of a potential issue when using in-line nebulizers in certain configurations with Trilogy Evo and Trilogy Ev300 devices. The use of in-line nebulizers placed in certain locations can result in aerosol deposits accumulating over time on the device's internal flow sensor. Impacted flow sensors may result in inaccurate flow measurements in certain circumstances. Recall start date: September 18, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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