Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | High |
| Status | ongoing |
| Recall date | March 02, 2026 |
| Reported | April 01, 2026 |
| Recalling firm | Philips Respironics, Inc. |
| Country / region | United States PA |
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.
Affected products
- Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.
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