Philips Respironics Recalls

4 recalls found for Philips Respironics. Check if any of your products are affected.

CRITICALFDA DEVICE

Philips Respironics Trilogy Evo O2 Ventilator Recall Covers 113,717 Units Worldwide (2026)

Philips Respironics recalled 113,717 Trilogy Evo O2 home-use ventilators worldwide on March 2, 2026 after determining that using non-pneumatic nebulizers with the device can cause a mismatch between the set tidal volume and the delivered tidal volume. The defect could lead to under- or over-ventilation with serious health consequences. Stop using the device immediately and follow the recall steps.

Philips Respironics
Using non-pneumatic
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HIGHFDA DEVICE

Philips Respironics Trilogy Evo Ventilators Recalled for Tidal-Volume Mismatch (113,717 Units, 2026)

Philips Respironics recalled 113,717 Trilogy Evo ventilators worldwide on March 2, 2026. The recall concerns software Version 1.05.15.00 and the use of non-pneumatic nebulizers with the Trilogy Evo platform. Hospitals and patients should stop using the device immediately and follow recall instructions from Philips Respironics or their healthcare provider.

Philips Respironics
Using non-pneumatic
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CRITICALFDA DEVICE

Philips Respironics Trilogy Evo Universal Ventilator Recall Affects 113,717 Units Worldwide in 2026

Philips Respironics recalled 113,717 Trilogy Evo Universal ventilators worldwide on March 2, 2026. The recall cites a condition where using non-pneumatic nebulizers may cause a discrepancy between the set tidal volume and the delivered tidal volume. Patients and caregivers should stop using the device immediately and contact Philips Respironics or their healthcare provider for instructions.

Philips Respironics
Using non-pneumatic
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HIGHFDA DEVICE

Philips Respironics Trilogy EV300 Recalled 113,717 Units Worldwide for Tidal Volume Discrepancy (202

Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold worldwide through healthcare distributors on March 2, 2026. Using non-pneumatic nebulizers with Trilogy Evo Platform ventilators may cause a mismatch between the set tidal volume and the delivered tidal volume. Patients and healthcare providers should stop using the device immediately and follow the recall instructions from the 제조

Philips Respironics
Using non-pneumatic
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Brand Statistics

Total Recalls
4
Pages
1