FDA DeviceClass INotable

FDA Recall: Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator devi

Name: FDA Recall: Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator devi
Brand: Philips Respironics, Inc.

Date: 2026-04-01

Brand: Philips Respironics, Inc.

Category: Medical Device

FDA Class: Class I

Description

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.

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.