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Philips Trilogy Evo Class I recall, tidal volume discrepancy

Favicon for changeflow.com FDA: Device Recalls Class I
Detected April 7th, 2026
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Summary

Philips Trilogy Evo Class I recall, tidal volume discrepancy

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Philips Respironics, Inc.

Device Recalls (Class I)

← All Device Recalls (Class I) Class I Z-1614-2026 · 20260401 · Ongoing

Product

Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.

Reason for Recall

Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.

Distribution

Worldwide distribution: US (Nationwide) and OUS (Foreign) to countries of: Argentina, Austria, Australia, Bosnia and Herzegovina, Bangladesh, Belgi...

Source: openFDA Enforcement API

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Source

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FDA: Device Recalls Class I changeflow.com/changebridge/fda-enforcement/device-class-i
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