FDAMarch 2, 2026device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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