RECALL INFORMATION
In June 2021, after discovering a potential health risk related to a part found within certain CPAP, BiPAP and Mechanical Ventilator devices, Philips issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).
Patient safety is our top priority, and we are committed to supporting our patients, durable medical equipment providers (DMEs), distributors, home health partners, and clinicians through the complete remediation process.
Throughout the remediation of this recall we will provide guidance and share next steps so you can ensure you have the most current and accurate information.