Philips CPAP & BiPAP Ventilator Recall Products Liability Litigation
Case Overview
In June 2021, Philips issued one of the largest medical device recalls in U.S. history, affecting approximately 5.5 million CPAP, BiPAP, and mechanical ventilator devices. The recall was triggered by the degradation of polyester-based polyurethane (PE-PUR) sound abatement foam used inside the devices. When the foam breaks down — accelerated by heat, humidity, and certain cleaning methods — it can release toxic and potentially carcinogenic particles and gases directly into the patient's breathing pathway. Users reported serious injuries including respiratory issues, headaches, and various cancers.
Thousands of lawsuits were consolidated into a multidistrict litigation in the Western District of Pennsylvania. In 2024, Philips agreed to a landmark settlement exceeding $1.1 billion to resolve personal injury claims, with a separate $479 million economic loss settlement also reached for device replacement costs. The case stands as one of the largest medical device mass tort settlements in recent history, drawing comparisons to the 3M earplug litigation in scale and complexity.
Who May Qualify
U.S. residents who used a recalled Philips CPAP, BiPAP, or mechanical ventilator device and suffered personal injuries — including respiratory illness, cancer, or other health conditions — potentially linked to PE-PUR foam degradation. Economic loss claimants who purchased or paid out-of-pocket for a recalled device may also qualify.
Frequently Asked Questions
Is the Philips CPAP lawsuit still open?
A major personal injury settlement of over $1.1 billion was reached in 2024. While the primary settlement claims deadline was October 29, 2024, some proceedings may remain ongoing. Affected users should consult an attorney or the official settlement website for current status.
What injuries qualify for the Philips CPAP lawsuit?
Users who developed respiratory illnesses, certain cancers (including lung and thyroid cancer), or other serious health conditions linked to the degraded foam in recalled Philips devices may qualify. You must have used one of the recalled CPAP, BiPAP, or ventilator models.
Which Philips CPAP models were recalled?
The recall covered numerous Philips Respironics devices, including the DreamStation, DreamStation 2, System One, REMstar, and several BiPAP and ventilator models. A full list is available on the FDA's website and the official settlement portal.