FDAMarch 1, 2023device

Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator, Model Numbers DS2100X11B, IN2100X15B, IN2100X19, FX2100X15B, JP2100X16B, AU2100X15B, LA2100X15B, CA2100X12B, CN2100X17B, BR2100X18B, KR2100X15B, IA2100X15B, PP2100X10, FP2100X10, FR2100X14B, ND2100X15B, IT2100X21B, ES2100X15B, DE2100X1...

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

The hazard

The accuracy of delivered oxygen may deviate below the required tolerance of 5% from setpoint when providing high concentration oxygen therapy. Additionally, if equipped, the internal FiO2 sensor may indicate a value higher than the device is actually delivering. This may lead to under delivery of oxygen.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

606959051997606959054059606959055575606959061019606959055599606959055636606959062085606959055643606959055650606959055438606959054097606959054103

Recall history

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

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