FDA MedWatch: Ventilator Correction: Philips Issues Correction for Trilogy Evo Platform Ventilators
Published: 04/16/2026
Sources:
- Food and Drug Administration
Relevant To:
- Ambulatory Surgical Centers,
- Rural Emergency Hospitals,
- Critical Access Hospitals,
- Home Health,
- Hospitals,
- Long Term Care
Philips has issued a letter to affected customers recommending all Trilogy ventilators be corrected prior to continued use. This includes Trilogy EVO, Trilogy EV300, Trilogy Evo O2, and Trilogy Evo Universal devices.
This recall involves correcting devices and does not involve removing them from where they are used or sold.
See full list of affected product
FDA Recommendations
Update all Trilogy Evo Platform ventilators with software version 1.05.15.00. Stop all use of non-pneumatic …
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