FDAMarch 1, 2023device

Trilogy EV300 Portable Electric Ventilator, Model Numbers DS2200X11B, IN2200X15B, FX2200X15B, CA2200X12B, CN2200X17B, BR2200X18B, KR2200X15B, IA2200X15B, FR2200X14B, ND2200X15B, IT2200X21B, ES2200X15B, DE2200X13B, BL2200X15B, GB2200X15B, EU2200X15B, EU2200X19, EE2200X15B, TR2200X15B, RU2200X15B

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

606959052017606959056497606959061033606959052321606959058613606959058620606959058644606959058668606959058675606959058682606959058705606959058798

Recall history

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

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