Philips A-Series BiPAP Lawsuit | 2025 Latest Updates

Philips Respironics is recalling its popular A-Series BiPAP Machine and numerous other CPAP and respirator devices after they were linked to an increased risk for severe health problems including cancer, prompting lawsuits nationwide.
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C.L. Mike Schmidt Published by C.L. Mike Schmidt

Philips A-Series BiPAP Lawsuit Overview

Thousands of plaintiffs have filed lawsuits against Philips Respironics claiming that the company’s sleep apnea machines caused severe health reactions ranging from respiratory issues to cancer. The primary allegations center around the use of an inferior sound abatement foam that deteriorates and releases dangerous chemicals and tiny particles into the lungs. The FDA has classified this as a Class I Recall, which is the most urgent and serious recall allowed by law. Class I Recalls pertain to defective products that can cause serious health problems or death.

Latest Philips A-Series BiPAP Lawsuit Updates

  • June 2022 – Philips released an update on its PE-PUR foam testing, stating that the levels of chemical gasses released by the foam weren’t expected to cause problems. The company continued to place blame on ozone cleaners, claiming the foam in Philips sleep apnea machines exposed to ozone cleaners was 14 times more likely to degrade. The FDA hasn’t released any new guidance or confirmed Philips’ findings [1].
  • December 2021 – SoClean filed an amended complaint that referenced the FDA’s report. According to the complaint, Philips knew for years that the foam could cause a “serious risk of harm,” but instead of warning the public, it engaged in a smear campaign against SoClean [2].
  • June 14, 2021 – Philips Respironics issued a recall notification in the United States for specific Continuous Positive Airway Pressure, BiLevel Positive Airway Pressure (BiLevel PAP) devices, and Philips Respironics ventilators. The sleep apnea machine recall came months after the company advised of a potential health risk related to its products [3].

Philips A-Series BiPAP Injuries & Side Effects

Users of recalled Philips A-Series BiPAP machines have reported a wide range of serious injuries and side effects related to foam degradation and chemical exposure:

  • Cancer (carcinogenic effects): Including blood cancers such as multiple myeloma and leukemia
  • Respiratory Issues: Lung scarring, pulmonary fibrosis, and breathing problems
  • Inflammatory Conditions: Sarcoidosis, inflammation, and chest pressure
  • Toxic Effects: Headache, irritation, and other health issues from chemical exposure

Do You Qualify for a Philips A-Series BiPAP Lawsuit?

You may qualify for a Philips A-Series BiPAP lawsuit if:

  • You used a recalled Philips A-Series BiPAP machine
  • You experienced serious side effects including respiratory issues, cancer, lung scarring, or other related health problems
  • The injuries required medical treatment or hospitalization
  • You can provide medical documentation linking your injuries to the BiPAP device

Evidence Required for a Philips A-Series BiPAP Lawsuit

To support your claim, you will need:

  • Medical records showing the health impacts of using the device
  • Proof of purchase or usage of the A-Series BiPAP Machine
  • Any communication with the manufacturer regarding the defect
  • Documentation of your recalled Philips machine (it’s important to keep the device for evidence)

Damages You Can Recover

Compensation in a Philips A-Series BiPAP lawsuit may include:

  • Medical expenses for treatment of injuries
  • Lost wages due to illness or treatment
  • Pain and suffering
  • Other related damages caused by the defective device

Understanding the Philips A-Series BiPAP Device

A Philips A-Series BiPAP Machine pumps air under varying pressure into the airway of the lungs. BiPAP machines use a higher pressure when you breathe in and lower pressure when you breathe out. These devices are commonly used to treat sleep apnea, a condition where breathing stops and restarts many times while you sleep.

There are two types of sleep apnea:

  • Obstructive sleep apnea – Occurs when your upper airway becomes blocked many times while you sleep, reducing or completely stopping airflow. Anything that could narrow your airway such as obesity, large tonsils, or changes in your hormone levels can increase your risk for obstructive apnea.
  • Central sleep apnea – Occurs when your brain does not send the signals needed to breathe. Health conditions that affect how your brain controls your airway and chest muscles can cause this kind of apnea.

FAQs

1. What health risks are associated with the A-Series Bipap Machine?

Health risks associated with the A-Series BiPAP machine include respiratory problems, headaches, and potential exposure to harmful chemicals due to defective components in the device.

2. Who can file a lawsuit regarding the A-Series Bipap Machine?

Anyone who has used the A-Series BiPAP Machine and suffered adverse health effects or damages related to its defects can file a lawsuit regarding the A-Series BiPAP machine. Consulting with a personal injury attorney is recommended.

3. What compensation might I be entitled to in the A-Series Bipap Machine Lawsuit?

Compensation that you might be entitled to in the A-Series BiPAP machine lawsuit covers medical expenses, lost wages, pain and suffering, and other related damages caused by the defective BiPAP machine.

4. How do I join the A-Series Bipap Machine lawsuit?

To join the A-Series BiPAP machine lawsuit, you must contact a personal injury attorney who specializes in product liability cases. They will evaluate your situation and guide you through the process of filing a claim.

5. What evidence do I need to support my claim in the A-Series Bipap Machine lawsuit?

The evidence you need to support your claim in the A-Series BiPAP machine lawsuit includes medical records showing the health impacts of using the device, proof of purchase or usage of the A-Series BiPAP Machine, and any communication with the manufacturer regarding the defect.

6. Is the Philips sleep apnea machine I used involved in the lawsuit?

This litigation involves sleep apnea devices included in the recall. Make sure you know the brand and model of your machine. If you aren’t sure if your breathing machine is a recalled sleep apnea machine or ventilator, an attorney can help you figure it out.

7. Should I keep my recalled Philips Sleep Apnea Machine?

It’s important to keep your recalled Philips machine for evidence in a potential case. Your lawyer can help you keep the machine if your supplier is asking you to return it.

Related Articles:

See all related medical device lawsuits our lawyers have covered.

Get a Free Philips A-Series BiPAP Machine Recall Lawsuit Evaluation With Our Lawyers

Time is limited to pursue legal action against Philips for defective A-Series BiPAP machines. If you or a loved one has suffered injuries from these recalled devices, it’s crucial to act quickly to protect your rights.

Our legal team offers:

  • Free, confidential consultations
  • No upfront costs or fees
  • Payment only if we win your case
  • Experienced representation in product liability cases

References:

  1. https://www.philips.com/a-w/about/news/archive/standard/news/press/2022/20220628-philips-provides-update-on-philips-respironics-pe-pur-sound-abatement-foam-test-and-research-program.html
  2. https://www.drugwatch.com/news/2021/12/16/soclean-cpap-lawsuit-philips-knew-products-created-serious-risk-harm/
  3. https://www.fda.gov/medical-devices/respiratory-devices/recalled-philips-ventilators-bipap-machines-and-cpap-machines

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