RECALLED PHILIPS CPAP, BIPAP, & VENTILATOR LAWSUITS
For years, millions of Americans suffering from sleep apnea and severe respiratory disorders relied on Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (BiPAP), and mechanical ventilators to help them breathe safely through the night. However, Philips Respironics, the industry’s largest manufacturer, controlling roughly 65% of the mechanical ventilator market. recalled an estimated 15 million devices after revealing a catastrophic design defect that turned these medical devices into severe health hazards.
The recall impacts popular product lines manufactured between 2007 and 2021, including the DreamStation series, SystemOne, and Trilogy ventilators. If you or a loved one used a recalled Philips breathing machine and were subsequently diagnosed with cancer, severe lung scarring, or chronic respiratory disease, you should not bear the financial and emotional burden alone. Stag Liuzza helps individuals and families across Louisiana and nationwide take aggressive legal action to hold negligent manufacturers accountable and secure the compensation required for extensive medical treatment.
What is Philips CPAP and mass tort litigation?
Philips CPAP and BiPAP litigation involves mass tort and product liability lawsuits against the manufacturer for designing and selling defective medical equipment. These claims allege that Philips utilized a dangerous, toxic sound-dampening insulation that disintegrates directly into the device’s air pathway, forcing users to inhale industrial chemical particles and toxic gasses every single night.
These cases seek substantial financial recovery for past and future medical expenses, permanent cellular and organ damage, lost earning capacity, and the immense pain and suffering endured by victims of consumer fraud. Facing a massive global corporation requires extensive legal resources and an unshakeable strategy. With the right representation, you can join the fight for accountability and secure your family’s future.
At Stag Liuzza, we understand that confronting a global medical manufacturing giant like Philips can feel incredibly daunting, especially while managing a serious chronic illness. Because product liability cases are highly time-sensitive, our legal team moves quickly to cut through corporate bureaucracy, track down your historical medical device records, and properly document your diagnostic history.
THE SCIENCE BEHIND THE HAZARD: PE-PUR FOAM DEGRADATION
- Particulate Inhalation and Ingestion: The foam fragments into tiny, microscopic black particles and debris. These chemical particles are blown directly into the machine’s air path, where the user unknowingly swallows or inhales them deep into their lungs.
- Chemical Off-Gassing: Beyond the visible debris, the degrading foam releases toxic, volatile organic compounds (VOCs) and gasses. Inhaling these industrial vapors exposes the user directly to aggressive, man-made carcinogens and cell-damaging toxins.
Because of the extreme risk of severe illness or death, the U.S. Food and Drug Administration (FDA) designated this a Class 1 Recall, the highest and most urgent level of consumer warning available.
MEDICAL COMPLICATIONS LINKED TO PHILIPS RECALLED DEVICES
ELIGIBILITY
Proving Corporate Knowledge and Negligence
The core argument in the nationwide litigation against Philips is that the manufacturer knew about the potential harm of their PE-PUR foam for years. Internal evidence suggests they deliberately withheld information about the foam’s toxic degradation to protect their corporate profits, only issuing a recall once they had an entirely new line of products ready to launch. This amounts to consumer fraud, design defects, and fraudulent concealment.
To build an unassailable product liability claim, our legal team conducts rigorous independent investigations and coordinates with expert medical witnesses to link your diagnosis directly to your device use. We assist you in gathering:
- Official proof of your prescribed Philips CPAP, BiPAP, or ventilator model (including serial numbers).
- Subsequent medical records explicitly documenting a qualifying cancer or severe respiratory diagnosis.
- Detailed history of your medical billing, prescription receipts, and lost wages due to illness.
UNDERSTANDING MASS TORT SETTLEMENTS & STATUTES OF LIMITATIONS
The legal fight against Philips has moved rapidly. A massive $1.1 billion master settlement was established to resolve personal injury claims and long-term medical monitoring for qualified U.S. citizens and residents who registered within the multidistrict litigation (MDL) frameworks. Additionally, separate multi-million-dollar economic loss class actions have been finalized to handle device replacement costs.
However, navigating these massive settlements requires an incredibly strategic approach. Most states carry a strict two-year statute of limitations for product liability and personal injury claims. Because Philips issued their initial recall notices in 2021, the legal windows for filing brand new independent claims are exceptionally tight and require immediate attention to determine if an exception applies to your case.
At Stag Liuzza, we don’t treat mass torts like a factory processing line. We recognize that behind every medical record is a human being facing a life-altering diagnosis. While mass torts allow for the shared benefits of a multi-billion-dollar corporate settlement, our firm ensures your individual pain, suffering, and prognosis are evaluated with the highest degree of personalized attention.
Why Choose Stag Liuzza As Your CPAP Mass Tort Lawyers?
Stag Liuzza is a nationally recognized law firm with a decorated history of taking on the world’s largest corporate polluters and manufacturing conglomerates. Our trial lawyers have helped recover billions of dollars in verdicts and settlements because we refuse to back down when massive insurance defense teams try to minimize human suffering.
We closely monitor the ongoing MDL dockets and the administrative requirements of the extraordinary injury funds. Our team coordinates directly with independent pulmonologists, lifecare planners, and toxicologists to build an airtight case that connects your exact device usage to your current health conditions.
Device victims who partner with Stag Liuzza benefit from:
- Billion-Dollar Trial Backing: We possess the deep financial resources required to fight multi-billion-dollar corporations on a level playing field.
- Elite Expert Coordination: We engage top-tier medical and scientific experts to prove design defects and chemical causation.
- Aggressive, Strategic Advocacy: We don’t just accept standard settlement structures—we push to ensure your specific, severe injuries are fully accounted for.
- Zero Upfront Fees: We operate strictly on a contingency-fee model. We handle all the upfront legal expenses, and you owe us absolutely nothing unless we secure a monetary recovery for you.
Results That Speak
In March 2024, 3M finalized a settlement of up to $12.5 billion for U.S. public water suppliers to address PFAS contamination. The agreement covers water systems with current or future detections of "forever chemicals," with funds supporting testing, filtration, and infrastructure improvements.
Jury verdict for property owners whose land was contaminated with radioactive materials from oil and gas operations.
Verdict for pipeyard worker who contracted lung cancer from exposure to Radium-226 and other radioactive materials.
Settlement for commercial auto injury case involving a large insurance company.
No fee unless we win. Past results do not guarantee similar outcomes.
Meet the Team
With decades of combined experience in environmental law, toxic torts, and complex litigation, Stag Liuzza's attorneys have the expertise to take on the most challenging cases.
Michael G. Stag
CEO & Managing PartnerOver $16 billion in settlements and more than $1 billion in jury verdicts recovered for clients. Pioneered the field of oilfield cleanup litigation. Appointed by judges to leadership for several nationwide litigations.
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Ashley M. Liuzza
COO & PartnerAppointed co-lead class counsel in major environmental cases. Extensive PFAS litigation experience. Helps people who developed meningioma as a result of being prescribed Depo-Provera.
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Merritt Cunningham
PartnerLeads the pharmaceutical and medical device division. Extensive MDL and mass tort experience. Represents thousands of firefighters harmed by PFAS exposure.
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Matthew D. Rogenes
PartnerPartner and trial lawyer. Trial and settlement experience in trucking cases and maritime personal injury. Recently recovered over $20 million for clients.
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If you or a loved one has been harmed by a CPAP machine, we’re here to help. Let’s discuss your case.
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365 Canal Street, Suite 2850
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