Thank you for your patience. Your DreamStation 2 device is provided to you as a replacement for your existing therapy device. This device has been inspected and is safe for your continued therapy use. Don’t forget to download the DreamMapper app to help track your progress, set goals and get helpful tips.
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 may have comparable settings to your previous device. If, however, you chose to receive a device with Auto-adjusting CPAP settings, it will be set to factory default. You can learn more about the differences between CPAP and Auto-adjusting CPAP here.
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.
While the DreamStation 2 was not affected by the PE-PUR recall, patients may have received one as a replacement for an affected sleep therapy device. If you have questions about the recent FDA notice, please contact customer service at 833-262-1871.
DreamStation Setting | DreamStation 2 Setting |
Tube Size | Matches DreamStation setting |
Ramp Pressure | Ramp Plus pressure set to off (patient to select desired starting pressure) |
NOTE: If you had a Ramp pressure set on your device, you will need to reset on the DreamStation 2 device using the replacement Ramp Plus feature. This can be adjusted by tapping the Ramp Plus icon while therapy is running and tapping the +/- icons until the desired and comfortable start pressure is achieved. After Ramp Plus is set, the device will automatically deliver this pressure during the therapy session and future therapy sessions without additional activation.
Using the packaging material that came with your replacement device, place your affected device in the shipping box provided. If applicable, please ensure your humidifier is empty of water.
Tape the box after packaging is complete. The tape should be centered so equal amounts of tape extend down the sides of the shipping box as shown here.
Peel the pre-paid label from its backing and attach it to the shipping box making sure you completely cover the original shipping label.
Ensure the shipping box is securely taped and sealed to prevent it from breaking open during shipment.
The guidance below is intended to address some of the more common questions we receive about replacement devices. If you cannot find what you are looking for, please call 833-262-1871 for additional support.
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:
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