About Philips CPAP Lawsuit
Philips CPAP and BiPAP machines were recalled in June 2021 due to degradation of the polyurethane foam in the sound abatement component. This foam break-down releases toxic particles and chemical compounds that users inhale directly into their lungs. Millions of patients using these devices for sleep apnea treatment were unknowingly exposed to harmful materials, potentially increasing cancer risk and causing respiratory injury.
Philips had internal knowledge that the foam could degrade and release particles, yet failed to adequately warn users or implement design changes. Patients using these devices for essential respiratory support during sleep faced accumulating exposure to toxic foam particles night after night. Some patients experienced immediate respiratory symptoms, while others faced increased cancer risk from chronic chemical exposure.
The recall affected millions of devices worldwide. While Philips offered repairs and replacements, many patients already suffered respiratory injury, lung inflammation, and other health effects. If you used a recalled Philips CPAP or BiPAP machine and developed respiratory problems, lung disease, or cancer, you may be eligible for significant compensation.