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Safety Recall Notice: Philips Respironics Medical Device Recall - CPAP, BiLevel PAP and Ventilators


On June 14, 2021, Philips Respironics announced a recall for certain CPAP, BiLevel PAP and Ventilator Devices due to two issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in these devices.

June 28, 2022 Updated Communication from Phillips Respironics

For information on the Recall Notice, a complete list of impacted products, potential health risks,  what to do if your device is affected, and how to register it, visit

ProResp is committed to providing you with effective PAP therapy in a patient-centred and safe manner that encourages long-term therapy compliance. To that end we are here to help you navigate through this recall. Please contact your local ProResp office for assistance.

We will update this page as more information becomes available.


Canadian Sleep Society

Health Canada – Recalls and Safety Alerts

Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (BiPAP), and Mechanical Ventilators (2021-06-14) - Recalls and safety alerts (