Philips Respironics recalled millions of CPAP, BiPAP, and ventilator machines after finding that the sound-dampening foam inside them could degrade and release particles and chemicals into the airway. Users diagnosed with cancer or a serious respiratory illness after use may qualify for compensation.
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In June 2021, Philips Respironics recalled millions of CPAP, BiPAP, and mechanical ventilator devices after determining that the polyester-based polyurethane (PE-PUR) foam used to reduce machine noise could break down over time — especially in heat and humidity — and release small particles and chemical gases directly into the pathway a user breathes from every night.
Users of the recalled devices have reported a range of health effects following prolonged use, from respiratory irritation to more serious diagnoses. These claims are filed against Philips and related manufacturers — not against the doctor who prescribed the device for a legitimate sleep or breathing condition.
Anyone who used a recalled Philips CPAP, BiPAP, or ventilator device — generally for six months or longer — and was later diagnosed with cancer, respiratory illness, or another condition potentially linked to foam degradation.
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Past and ongoing treatment related to your diagnosis.
Time away from work during treatment or recovery.
The physical and emotional impact of your diagnosis.
No. The case review is free, and if a network attorney takes your case, they're paid a percentage of any settlement or award — never a fee up front.
A network attorney can help you check your device's model and serial number against the official recall list during your free review — you don't need to have already confirmed this yourself.
Any decision about your device or treatment should be made with your doctor, not based on this page. This review is about whether past use may support a compensation claim.
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