The DreamStation 2 AutoCPAP Advanced was designed with your comfort and ease in mind. It is easy to use and features a Ramp Plus setting that will allow you to pick a starting pressure that is comfortable to help you fall asleep. We understand that any change to your therapy device can cause concern. We are working with your homecare provider/DME to ensure proper and smooth replacement device setup. We have a patient management software solution that in many cases allows your homecare provider to access the prescription settings from your previous device. This means your replacement device will have comparable settings to your previous device. Don’t forget to download the DreamMapper app to help track your progress, set goals and get helpful tips.
While affected devices contained a polyester-based polyurethane (PE-PUR) sound abatement foam component, the sound abatement foam in all new and recertified devices is a silicone foam that has met all applicable industry testing standards, including particulate and Volatile Organic Compounds (VOCs) emissions testing, and is authorized as part of our remediation.
Philips DreamStation 2 Auto CPAP Advanced Menus and Comfort Features for Patients
Before resuming therapy on your new or replacement machine, you or your equipment provider must visually inspect the following accessories for evidence of particulate contamination: If there is no evidence of particles on any of these components: If visible particles are evident on any of these components:
Philips DreamStation 2 Auto CPAP Cleaning and Maintenance
Upon receipt of Advanced Exchange, please follow the instructions that you receive regarding the return of your Affected Device to Philips. Specifically, it is important that you promptly return your Affected Device. Your returned Affected Device will either be repaired to replace the foam insulation with an approved insulation, or will be destroyed.
Please note that in order to effectuate the Recall Plan it is necessary that you return your Affected device promptly, consistent with FDA regulations. By participating in the Advanced Exchange or receiving a remediated device, you acknowledge and agree that the foam insulation will be removed and may be discarded, and that your Affected Device may be destroyed or refurbished. Thank you again for your assistance in this matter.
You are about to visit a Philips global content page
Continue