FDAJuly 16, 2024device

Trilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL2110X15B Trilogy Evo, Benelux BR2110X18B Trilogy Evo, Brazil CA2110X12B Trilogy Evo, Canada DE2100X13B Trilogy Evo O2, Germany DE2110X13B Trilogy Evo, Germany DS2100X11B Trilogy Evo, O2, USA DS2110X11B Trilogy Evo, US...

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

The hazard

Firm has released a mandatory software update Version 1.05.10.00 and a User Manual addendum for affected ventilators. These updates resolve safety issues identified in earlier recalls.

What to do

FDA enforcement status: Ongoing

Brands named

philips respironicsphilips

UPCs

606959051980606959055520606959055476606959052307606959054103606959054110606959051997606959051942606959055698606959055544606959054097606959054080

Recall history

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

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