Philips Respironics Recall Notice

On June 14, 2021, Philips Respironics issued a voluntary recall notification for their Continuous Positive Airway Pressure (CPAP) and Bi-Level Positive Airway Pressure (Bi-Level PAP) machines due to potential health risks related to the sound abatement foam used in their respective devices. 

For information on the recall notice, a complete list of impacted products, and potential health risks, visit www.philips.com/src-update

We encourage you to speak to your physician should you have any other questions relating to the recall and your therapy.

We regret any inconvenience caused by this Philips Respironics recall. Please call us at (800) 673-1220 if you would like to speak with one of our representatives or email us at info@cpapnation.com.

As we learn more, including updates from Philips Respironics on their repairing or replacing of affected machines, we will update this notice.  

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