Philips is a renowned brand based in Amsterdam that specializes in the production of cutting-edge sleep and respiratory care devices. Their range of products includes CPAP, BiPAP, and mechanical ventilator devices designed to provide optimal care and support for patients. However, in June 2021, Philips discovered a potential health risk related to the foam in certain devices and took immediate action by issuing a voluntary recall notification in the U.

S. This recall affects a specific range of devices manufactured before April 26, 2021. Despite this setback, Philips remains committed to delivering the best care possible.

They have produced a significant number of new devices and repair kits to meet the demand and have already remediated a large portion of affected devices, ensuring they are in the hands of patients and durable medical equipment providers. Furthermore, Philips advises against using ozone and UV light cleaning methods for their sleep apnea devices or masks, as they are not currently approved. Throughout the remediation process, Philips is dedicated to supporting patients, business customers, and clinicians.

They continue to provide updated information and remain focused on resolving the issue and restoring trust. As a brand, Philips prioritizes patient safety and is working diligently to address the situation and provide the best solutions in sleep and respiratory care