Philips CPAP Lawsuit: A Comprehensive Guide (2024)

What is the Philips CPAP Lawsuit?

Continuous Positive Airway Pressure (CPAP) machines are some of the most commonly used treatments for obstructive sleep apnea, a condition characterized by intermittent breathing pauses during sleep. According to the National Council on Aging (NCOA), the condition affects approximately 39 million adults in the United States.

Philips CPAP machines, designed and marketed by Philips Respironics – some of the leading and longest-standing CPAP manufacturers – are among the most widely recognized in the healthcare industry.

History of Philips CPAP

Since its inception in 1976, Philips Respironics has been at the forefront of innovation in sleep and respiratory care. Their CPAP machines cater to those suffering from sleep apnea, offering a variety of models that range from basic designs to more advanced units with humidification systems and mobile connectivity.

Historically, Philips CPAP machines are held in high regard due to their effectiveness, reliability, and user-friendly features. Through continuous research and development, Philips Respironics has strived to meet the evolving needs of CPAP users, prioritizing both comfort and therapeutic efficacy.

What Are the Issues with Philips CPAP?

Despite their reputation, Philips CPAP machines have recently faced scrutiny. Concerns emerged when Philips Respironics issued a voluntary recall announcement in 2021. The recall affected millions of units and pertained to PE-PUR sound abatement foam used in Philips Continuous and NonContinuous Ventilators that could degrade. The recall also warned that the PE-PUR foam may off-gas certain chemicals.

Deterioration of the foam, due to various factors including unapproved cleaning methods and high heat and humidity environments, can lead to potential health risks due to the release of a known carcinogen and respiratory irritant called formaldehyde. Users might inhale or ingest toxic foam particles or certain chemicals, potentially causing harm. The U.S. Food and Drug Administration (FDA) also alerted users of Philips CPAP machines of the health risks associated with breathing in or swallowing pieces of foam and certain chemicals.

From April 2021 to September 2023, the FDA received a total of 115,000 medical device reports and 561 reports of death caused by the PE-PUR foam breakdown.

Why Are People Filing Philips CPAP Lawsuits?

In the wake of the recall, numerous individuals affected by the foam degradation issue have initiated legal action against Philips Respironics. The lawsuits allege that Philips Respironics failed to disclose timely information about the foam degradation risks, leading to users unknowingly inhaling harmful substances.

The plaintiffs in these cases claim a variety of health issues attributed to the faulty CPAP machines, ranging from respiratory complications to organ damage and cancer. They seek compensatory damages for medical costs, suffering, and other related losses.

If you used a Philips CPAP and developed health complications caused by the machine, our team at ConsumerShield can connect you with legal experts so you can discuss your options to pursue a Philips CPAP lawsuit and recover compensation.

Philips CPAP Lawsuit Symptoms

For countless individuals relying on Philips CPAP and BiPAP machines, understanding the potential risks and recognizing the signs of exposure to the degraded foam has become paramount.

The sound abatement foam, designed to reduce noise and vibrations in the machine, has been identified as the main culprit behind the recall. As this foam breaks down, it can release particles and gasses that users might inadvertently inhale or ingest, posing a range of health concerns.

Key Symptoms of Exposure:

Breathing Difficulties

One of the most immediate and concerning symptoms users reported is trouble breathing. This can range from shortness of breath to more severe respiratory complications. Given that these machines are specifically designed to aid breathing, any respiratory issues experienced while using them should be taken very seriously.

Headaches

Persistent and unusual headaches, particularly those that develop after using the CPAP or BiPAP machine, can be an indicator of exposure to the degraded foam's harmful substances.

Dizziness

Some users have reported feeling dizzy or lightheaded, especially after waking up. This symptom might be linked to the inhalation of toxic chemicals released by the foam.

Other Related Medical Complications

Beyond the primary symptoms, users should be vigilant about other potential health issues, such as skin, eye, and throat irritation, nausea, or even systemic reactions. Each individual's response can vary, making it essential to monitor any unusual health changes closely.

If you suspect you've been exposed to harmful substances from a Philips CPAP or BiPAP machine, the first step is to seek medical advice immediately. Documenting your symptoms and any medical interventions can be crucial for your health and any potential legal actions you might consider.

In this challenging landscape, ConsumerShield offers a valuable resource for affected individuals. By providing free claim reviews, they connect users with legal experts who can provide guidance, ensuring victims' rights are upheld and they receive the support they need.

Philips CPAP Lawsuit Eligibility & Requirements

With the Philips CPAP recall capturing headlines and affecting millions, there's a growing need for clarity around who might be eligible to join the class action lawsuit.

A class action lawsuit is a legal action where a group of people, who have suffered similar harm by the same entity, collectively bring a claim to court. In the case of the Philips CPAP recall, the harm is believed to be caused by potential carcinogen and toxic chemical exposure from the devices.

Criteria for Qualification:

Ownership of a Recalled Device

The primary qualification criterion is the ownership or use of a recalled Philips CPAP, BiPAP, or ventilator machine. It's crucial to verify the model and brand of your device.

Documented Health Issues

Having medical records indicating health complications or symptoms believed to be linked to the device can strengthen a claim. These might include cancer, lung problems, breathing difficulties, or other related injuries.

Usage Duration

The length of time a patient used the device could play a role in eligibility. Those who used the device for extended periods might have a higher risk of exposure and subsequently a stronger claim.

Retaining the Device

Keeping the recalled device can be essential. It might be used as evidence, especially if testing is required to determine the presence of harmful chemicals.

Timelines

Legal actions are bound by statutes of limitations, which means claims need to be filed within a specific timeframe from when the injury was discovered or should have been discovered.

If you believe you might qualify but are uncertain about the specifics or the strength of your potential claim, ConsumerShield offers invaluable assistance. Their free claim review service provides clarity for potential victims, assessing the merit of their claims and guiding them on the next steps. Through ConsumerShield, affected individuals can also connect with expert legal teams who can advise them further and represent their interests in the lawsuit.