FDAMarch 19, 2024device

Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.

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

The hazard

Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.

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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