Medical Device Recall Notification – Philips Respironics Sleep and Respiratory Care Devices

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.

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