Trilogy EVO and EV300
In plain language
This recall involves Trilogy EVO and EV300 ventilators sold in Canada. They are being recalled due to issues with using non-pneumatic nebulizers and aerosol deposition on the internal flow sensor. Philips Respironics no longer permits the use of non-pneumatic nebulizers with these ventilators. This recall is for healthcare industry professionals.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Trilogy EVO
Model: CA2110X12B
Lot: Not applicable.
Trilogy EV300
Model: CA2200X12B
Lot: Not applicable.
Why this matters
Device compatibility issue
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: Not applicable.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: CA2110X12B, CA2200X12B
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Device compatibility issue
What should consumers do?
Contact the manufacturer if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Device compatibility issue
When was this product recalled?
This product was recalled on February 13, 2026.
Is the Respironics Inc. brand affected by this recall?
Yes, Respironics Inc. products are affected by this recall. This recall involves Trilogy EVO and EV300 ventilators sold in Canada. They are being recalled due to issues with using non-pneumatic nebulizers and aerosol deposition on the internal flow sensor. Philips Respironics no longer permits the use of non-pneumatic nebulizers with these ventilators. This recall is for healthcare industry professionals.