On June 14, 2021, Philips issued a recall notification for 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 this issue. Read below to learn more about the recall, determine if your device is impacted, and next steps to register your device. Call 1-877-907-7508 if you cannot visit the website or do not have internet access. With more questions or concerns regarding this Recall please call your PCP or the Durable Medical Equipment company in which you got your device from.
https://www.usa.philips.com/healthcare/e/sleep/communications/src-update
