The Recall: What to do
As you may have heard, yesterday Philips Respironics issued a recall of all DreamStation Auto CPAP and BiPAP machines due to a potential health risk posed by the foam used for sound abatement. The recall affects the original DreamStation devices but not the new DreamStation 2 that just became available in April of this year.
We have received several calls on this issue, our recommendation is to not use the device if:
Black debris are present in the air outlet, water reservoir, or hose
You experience upper airway irritation, cough, sinus infection, headache, nausea, or chest tightness.
You have underlying cardiopulmonary disease(s)
You have mild to moderate obstructive sleep apnea.
On the other hand, if your obstructive sleep apnea is severe, e.g. unable to sleep without the CPAP due to choking, gasping, waking up frequently, then you may continue using the machine as the benefits outweigh the risks in this case. If you do choose to continue with usage, an antibacterial filter may provide some benefits in blocking the particles. Although, the volatile organic compounds could still get though.
Philips Respironics is working on replacing the sound abatement foam in the CPAP. You will first have to register your CPAP online at www.philips.com/SRC-update. The website will guide you through the process and provide more information on the issue. You may also call 877-907-7508.
At Sound Sleep Clinic we apologize for the confusion from this inconvenience. If there are any questions, please do not hesitate to reply to this email or contact us at helpdesk@soundsleepclinic.com.
Most machines sold by Sound Sleep Clinic are relatively new as we have just started selling them a little over a year ago. Therefore, the foam piece is less likely to deteriorate when compared those in older devices.