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Philips Respironics, Inc.

Philips Respironics, Inc.: 2 recalls listed since March 2026 across FDA; 2 rated high risk.

By year

  • 20262

By agency

  • FDA2

By category

  • Medical Device2

All recalls (2)

Philips Respironics Trilogy EV300, Evo, Evo O2, and Evo Universal

In some situations, the Obstruction Alarm does not trigger within the timeframe dictated by the relevant standards and may take up to four breaths.

High risk, FDA, , Device defect

Philips Respironics Trilogy Evo Ventilators

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.

High risk, FDA, , Device defect
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