Official recall notice
FDA DeviceClass INotable
FDA Recall: Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilat
- Recall date
- 2026-04-01
- Category
- Medical Device
- FDA class
- Class I
Why it was recalled
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.
Recommended action
What to do
113717
Product 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.