Medical Device

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

Recall date: 2026-04-01 · Source: FDA_DEVICE

Brand / Firm

Product

Reason for recall

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.

Units affected

113,717 units

Description

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

View official recall notice →