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Philips Respironics, Inc. Recall

Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.

Updated March 2, 2026

Philips Respironics, Inc. is recalling Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.. Hazard: Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.

Is the Philips Respironics, Inc. recalled? Yes. This product was recalled by FDA on March 2, 2026. Details below.

What is recalled

Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may result in a discrepancy between the set tidal volume and the tidal volume received by the patient.

Brands affected

Philips Respironics, Inc.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-1616-2026
Classification
Class I
Recalled
March 2, 2026
Read the official notice

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