Skip to main content
Philips CPAP and BiPAP Recall Frustrates Millions of Sleep Apnea Patients

Philips CPAP and BiPAP Recall Frustrates Millions of Sleep Apnea Patients

Philips Continuous Positive Airway Pressure (CPAP) and Bi-Level Positive Airway Pressure (BiPAP) machines used by millions of people to manage sleep apnea have users worried after a Class I (the most serious type) recall was issued in June 2021. Certain sleep apnea machines and  ventilation devices manufactured by Philips were recalled by the company amid concerns over potential risks related to sound abatement foam used in specific CPAP and ventilator devices. Users may have inhaled cancer-causing toxins and off-gas chemicals caused by degradation of the foam. Conditions such as lung, kidney, or liver cancer and heart attacks may result from inhalation of these materials.

Are You Eligible to File a Philips CPAP Lawsuit?

If you or a loved one believe your condition is a result of using a Philips CPAP, BiPAP or mechanical ventilator, contact our experienced lawyers today.

Call us at (888) 984-7988 or fill out our contact form to schedule a free consultation. Grant & Eisenhofer, P.A. represents clients nationwide and is located at 123 Justison Street Wilmington, DE 19801. Other offices in Chicago IL, Baltimore MD, New York NY, and San Francisco CA. Attorney Advertising. Prior results do not guarantee a similar outcome.
https://www.gelaw.com/disclaimer/