medical HIGH RISK Updated 2026-04-01

Philips Respironics, Inc. recalls Philips Respironics Trilogy EV300, Software Version 1.05.15.

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Recalled Product

Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All Model No.; All UDI; All Serial No.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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View official government recall

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