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

PHILIPS RESPIRONICS MEDICAL DEVICE RECALL NOTIFICATION

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.

For information on the Recall Notice, a complete list of impacted products, potential health risks, and what to do if your device is affected visit philips.com/src-update.

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.

RELATED LINKS:

Canadian Sleep Society

https://css-scs.ca/phillips-respironics-positive-pressure-device-recall/

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 (healthycanadians.gc.ca)