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Health Canada Medical devices

Trilogy Evo and Trilogy Ev300

Issued October 2, 2024
Issue
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
Hazard description
Performance
Product
Product name
Trilogy Evo and Trilogy Ev300
Reference
ID
RA-76234