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Trilogy evo and trilogy ev300
Official notice
2 Oct 2024
Last checked
2 Oct 2024
An official Health Canada notice concerns Trilogy evo and trilogy ev300. 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 Published 2024-10-02.
What to do now
Contact the manufacturer if you require additional information.
Recall number
76234
Official notice
2024-10-02
The hazard
The hazard
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
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Affected products
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Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Philips, Trilogy Evo And Trilogy Ev300.
Source & status
Source & status
Source
Tier
Category
Classification
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Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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