In 2021, Philips recalled over 5 million CPAP, BiPAP, and mechanical ventilator devices because the PE-PUR sound abatement foam can degrade and release toxic particles and gases into the user's airway. These particles are known carcinogens and have caused cancers and respiratory damage.
Free Case EvaluationYou may qualify if you used a recalled Philips DreamStation, System One, or BiPAP device and were diagnosed with cancer or suffered respiratory damage.
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