On June 14, 2021 Philips issued a recall notification in the United States for specific affected ventilation and sleep apnea devices.
The notification informs patients, users and customers of potential impacts on patient health and clinical use related to an issue with the foam used for sound abatement.
If you own a Philips sleep apnea device sold before June of 2021, please visit the Philips website to learn more about your options and be sure to call our office to discuss alternative therapies.
https://www.usa.philips.com/healthcare/e/sleep/communications/src-update
