Attention patients using Philips Respironics CPAP, BiPAP, and Ventilation devices

Philips Respironics has issued a voluntary medical device recall notification (U.S. only) / field safety notice (Outside of U.S.) affecting specific Philips Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (BiLevel PAP) devices, and Mechanical Ventilators.

Philips has advised of potential health risks related to sound abatement foam used in the above mentioned devices and gives further information on potential impacts to patient health and possible health risks.

For more information, a detailed explanation of which devices are affected, next steps and FAQ’s please refer to the Philips Respironics website by clicking here:  https://www.usa.philips.com/healthcare/e/sleep/communications/src-update or by calling Philips Respironics at (877) 907-7508. You may also review this video for the proper procedure for registering recalled Philips Respironics devices.

Please know that Norco is focused on your safety, health and wellbeing.  We understand that this is difficult news for many of our valued customers.  We are in close contact with Philips Respironics and are awaiting further updates and action steps from Philips Respironics and/or the FDA. 

You can watch for the latest Philips Respironics Recall updates on their website:  https://www.usa.philips.com/healthcare/e/sleep/communications/src-update