Philips CPAP Pancreatic Cancer Lawsuit [2024 Update]

Recalled Philips CPAP Devices Potentially Linked to Pancreatic Cancer

Philips CPAP devices have been found to off-gas potentially carcinogenic substances due to the degradation of polyurethane foam used for sound abatement.

This foam, when it breaks down, can release volatile organic compounds (VOCs) such as toluene diamine (TDA), toluene diisocyanate (TDI), diethylene glycol (DEG), and dichloromethane (DCM).

Users of these devices may be at an increased risk of cancer due to chronic exposure to these chemicals, which may lead to cellular damage and mutations.

Specifically, pancreatic cancer may be linked to these devices through the systemic absorption of carcinogens that cause genetic mutations or disrupt normal cellular functions in the pancreas.

Pancreatic cells, due to their metabolic functions, may be particularly susceptible to disruptions caused by these chemicals.

The ongoing investigations and lawsuits aim to address these serious health concerns potentially linked to the Philips CPAP machines, BiPAP machines, and Ventilator devices.

If you were diagnosed with pancreatic cancer or other related health problems after using a Philips Respironics device, you may be eligible to file a CPAP Lawsuit.

Contact the Philips CPAP Lawyers at TorHoerman Law for a free consultation and to learn about your legal options.

You can also use the chatbot on this page for an instant case evaluation.

About Pancreatic Cancer

Pancreatic cancer is a type of cancer located in the pancreas, a vital organ involved in digestion and blood sugar regulation.

Pancreatic cancer is particularly dangerous because it often goes undetected until it’s in an advanced stage, which makes it particularly lethal and difficult to treat effectively.

Pancreatic cancer is one of the most deadly forms of cancer, with a five-year survival rate of about 12%.

An Overview of the Philips Recall on Sleep Apnea Devices

The 2021 Philips CPAP recall affected millions of the company’s sleep apnea devices, including CPAP machines, BiPAP devices, and mechanical ventilators.

The recall was initiated due to the discovery that polyester-based polyurethane (PE-PUR) sound abatement foam used in the devices could degrade and potentially release harmful chemicals and toxic foam particles.

According to the US Food and Drug Administration (FDA), the agency has received more than 116,000 medical device reports of foam breaking down in Philips CPAP and BiPAP machines.

In February 2024, the FDA also reported that within those 116,000 medical device reports were also 561 reports of death.

What Philips Devices are Recalled?

The June 2021 recall covered several different types of Philips Respironics devices, all claimed to suffer from the same defects.

Recalled devices were distributed between 2009 and April 26, 2021.

Recalled Philips CPAP products include:

• Philips Bi-level Positive Airway Pressure (Bi-Level PAP)
• Philips Continuous Positive Airway Pressure (CPAP)
• Certain Philips Respironics Ventilators

According to Philips’ recall announcement, recalled Philips CPAP machines include:

• Philips Bi-level Positive Airway Pressure (Bi-Level PAP)
  • A-Series BiPAP A30
  • A-Series BiPAP A40 (ventilator)
  • A-Series BiPAP Hybrid A30
  • A-Series BiPAP V30 Auto (ventilator)
• Philips Continuous Positive Airway Pressure (CPAP)
  • C-Series ASV (ventilator)
  • C-Series S/T and AVAPS
  • DreamStation
  • DreamStation ASV
  • DreamStation Go
  • DreamStation ST, AVAPS
  • C-Series ASV (ventilator)
  • C-Series S/T and AVAPS
  • Dorma 400
  • Dorma 500
  • OmniLab Advanced+
  • REMstar SE Auto
  • SystemOne ASV4
  • SystemOne (Q-Series)
• Other mechanical ventilator devices
  • E30
  • Garbin Plus, Aeris, LifeVent (ventilator)

Philips also recalled certain Trilogy Evo ventilators distributed from April 15, 2021 to May 24, 2021 with specific serial numbers (Trilogy 100 and 200).

Philips CPAP Lawsuit Overview

Philips Respironics is facing hundreds of personal injury and wrongful death lawsuit claims.

These cases are being consolidated into the Philips CPAP Recall MDL, which is centralized in the US District Court for the Western District of Pennsylvania.

This federal court is handling all personal injury claims related to the recalled Philips CPAP machines, BiPAP machines, and Ventilator devices.

For more updates on the Philips CPAP Litigation, visit this page.

Is There a Philips CPAP Class Action Lawsuit?

Yes, there is a a Philips CPAP Class Action Lawsuit to reimburse those who purchased recalled CPAP devices.

The Philips CPAP Class Action Lawsuit was settled for nearly $500 million.

The Philips CPAP Lawsuit involving personal injury claims and wrongful death potentially resulting from the use of recalled Philips CPAP devices is ongoing and has not yet been resolved.

As mentioned above, personal injury claims and wrongful death lawsuits involving defective CPAP, BiPAP, and ventilator devices are consolidated into the Philips CPAP MDL.

Multidistrict litigation (MDL) is a federal legal procedure designed to increase efficiency and promote consistency across cases that contain similar issues and circumstances.

MDL is different and distinct from a class action lawsuit.

In MDLs, each case is still treated individually, allowing for personalized settlements based on the specific damages of each plaintiff.

In a class action lawsuit, all claims are processed in a single lawsuit with compensation distributed among all class members according to predefined criteria, which may not account for individual variations in damages.

What is the Average Philips CPAP Settlement Amount?

There has not been a settlement in the Philips CPAP Lawsuit for personal injury claims and wrongful death cases.

However, attorneys estimate that the average Philips CPAP Lawsuit payout per person may range from $50,000 to potentially over $500,000 per person.

These settlement projects for personal injury claims related to the Philips CPAP devices are merely estimations based on prior mass tort lawsuits and are by no means a guarantee of compensation in the Philips CPAP Lawsuit.

It is essential to contact an experienced lawyer to understand your legal options and potential avenues for compensation in your case.

Reach out to TorHoerman Law for a free consultation.

You can also use the chatbot on this page for an instant case evaluation and to get in touch with our Philips CPAP Lawyers.

What is the Statute of Limitations for Philips CPAP Lawsuits?

The statute of limitations for Philips CPAP Lawsuits varies depending on the state where the lawsuit is filed, as each state has its own laws governing the timeframe in which a claim must be brought.

Most states have a product liability lawsuit statute of limitations of 2 (two) years.

Generally, this timeframe starts when the plaintiff discovers or should have discovered the injury and its potential link to the Philips CPAP device.

For many, this period may begin from:

• The date of the recall announcement (June 2021)
• When the user first experienced adverse effects.

It’s crucial to consult with a lawyer to determine the specific statute of limitations applicable to your case, as missing the deadline can bar you from filing a lawsuit.

Contacting a lawyer experienced in medical device litigation soon after discovering a potential injury can help ensure that your legal rights are preserved.

Do You Qualify for the Philips CPAP Recall Lawsuit?

Hundreds of CPAP Recall Lawsuits filed against Philips claim that defective sleep apnea machines produced by the company have caused health problems and potentially cancer.

Our lawyers are currently accepting new clients for the lawsuit.

If you used a device included in the Philips CPAP machine recall and subsequently developed cancer or other health issues, you may be eligible to file a Philips CPAP Lawsuit.

Reach out to a Philips CPAP Lawyer today from TorHoerman Law for a free consultation.

Use the chatbot on this page to find out if you qualify for the Philips CPAP Recall Lawsuit instantly.

Gathering Evidence for the Philips CPAP Machine Lawsuit

Evidence is extremely important in personal injury cases for defective and dangerous medical devices.

Your lawyer can help you gather and retain key evidence, but this is a step you can potentially start on your own.

Possible evidence in Philips CPAP Lawsuits includes:

• Medical records
• Prescription records (if you were prescribed CPAP therapy)
• The recalled device itself
• Medical device reports
• Information on your recalled Philips CPAP Machine
• Notes from your doctor
• Any other proof of Philips CPAP use and subsequent injury

Assessing Damages for the Philips CPAP Lawsuit

Damages are the total amount of losses, economic and non-economic, incurred as a result of using and being injured by a Philips CPAP, BiPAP, or Ventilator device.

Your lawyer can help assess and calculate damages in your case, seeking full and adequate compensation for how you have suffered.

Possible damages in an individual Philips CPAP Lawsuit may include:

• Medical expenses and medical bills
• Pain and suffering
• Emotional damages
• Lost wages
• Lost earning ability
• Permanent disability
• Loss of consortium
• Other compensatory and punitive damages

TorHoerman Law: Your Philips CPAP Lawyers

Defective CPAP machines made by Philips Respironics are potentially linked to serious health problems and potential cancer diagnoses in hundreds of CPAP users.

Our law firm is currently investigating Philips CPAP Injury Lawsuits, aiming to secure significant financial compensation for CPAP users who have developed cancer or other health issues.

If you used a device included in the Philips CPAP machine recall and subsequently developed pancreatic cancer or other health issues, you may be eligible to file a Philips CPAP Lawsuit.

Reach out to a Philips CPAP Lawyer today from TorHoerman Law for a free consultation.

Use the chatbot on this page to find out if you qualify for the Philips CPAP Recall Lawsuit instantly.