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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