Philips Respironics CPAP, BiPAP, and Ventilator Recall: FAQs

The FDA is providing answers to frequently asked questions related to this recall.

If your email program has trouble displaying this email, view as a webpage. Philips Respironics CPAP, BiPAP, and Ventilator Recall: Frequently Asked Questions The U.S. Food and Drug Administration (FDA) has posted answers to frequently asked questions related to Philips Respironics' recent voluntary recall of certain CPAP, BiPAP, and ventilators due to potential health risks. Check this resource to get answers to questions, including: I use one of the affected devices daily. I can't wait for a new device. What can I do now? When a medical device is recalled, what is the FDA's role? I understand the sound abatement foam may be causing the problems related to the recall. Should I try and remove the foam from my device?  Read More

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