Connect your DreamStation Your DreamStation has built-in support for Bluetooth which will connect to your mobile device and transfer your therapy results. Since solutions for the recall are almost as personalized as individual pressure settings themselves, its important to have a discussion with your doctor as soon as possible to determine the next steps. 6. Login with your Username and new Password. The initial concern with the foam related to possible emission of particulates (tiny particles) from degraded foam and certain chemicals of concern, called volatile organic compounds (VOCs). Below is the information you need to know on this recall, how you might be impacted, what next steps should be taken, and what you should expect. Many dealers expect to run out and go through at least intermittent back order periods for the foreseeable future. Additionally, we remind both customers and patients to review the age of their BiLevel PAP and CPAP devices, as they are recommended to be replaced after five years of use. To confirm that your Philips PAP device has been recalled, you need to visit the Philips registration site to register your device. Register your product and start enjoying benefits right away. Register your product and enjoy the benefits. As a result, testing and assessments have been carried out. Whether you choose to buy a machine outright or through your insurance company or pursue options through a government assistance program or donation initiative, CPAP.com is here to help you navigate the CPAP recall. If you already have a DreamMapper account but do not remember your Username, please note that your Username is your email address. CPAP.com is a family-owned and operated business dedicated to providing affordable sleep apnea equipment to those who need sleep therapy. To register your product, youll need to log into your MyPhilips account. Click Next. Philips Respironics Sleep Apnea Care If you do not remember your DreamMapper password or need to reset it: Click Forgot your password?. The CPAP team strives to provide insightful and meaningful information to its audience, keeping you in the know on the latest happenings in the sleep health and respiratory world. Many of the Philips Respironics CPAP, APAP, and BiPAP machines sold from 2009 onward except the DreamStation 2 used this type of sound abatement foam and are impacted by this recall. Philips Respironics offers innovative products for sleep and home respiratory care as well as medical education and value-added programs to help you navigate a rapidly changing industry landscape, and in the interest of maximizing both clinical and business success. Proof of purchase may be required to take advantage of a promotion or request a repair within warranty. This recall was announced on June 14, 2021. The initial concern with the foam related to possible emission of particulates (tiny particles) from degraded foam and certain chemicals of concern, called volatile organic compounds (VOCs). We recommend you upload your proof of purchase, so you always have it in case you need it. Accept terms and conditions. Dont have one? Click Submit to create your account. Koninklijke Philips N.V., 2004 - 2023.
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