FDAOctober 7, 2024device

Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for invasive and non-invasive ventilation of pediatric through adult patients weighing at least 2.5 kg in institutional, home, and non-emergency transport settings.

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

The hazard

Potential for in-line nebulizer configuration in certain locations to result in aerosol deposit accumulation on the device's internal flow sensor, which could lead to inaccurate flow measurements.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

606959052000

Recall history

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

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