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.
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 phillips.com/scr-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