FDAMarch 2, 2026device

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

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

The hazard

In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.

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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