On June 14, 2021, Philips Respironics issued a voluntary recall on specific brands of their continuous positive airway pressure (CPAP) machines, bi-level positive airway pressure (BiPAP) machines and ventilators. Philips Respironics has established a registration process that allows patients, users or caregivers to look up their device's serial number and initiate a claim if their unit is affected. To view the recall information and register your device, please visit the Philips Respironics website.
For questions, please call Philips Respironics at 877-907-7508. It is highly recommended that devices be registered to appropriately identify all recalled units and so that impacted patients, users and caregivers receive the most up-to-date information from Philips Respironics.