Recalled Philips CPAP Machines May Be Linked to Kidney Cancer

Kidney cancer may be linked to defective Philips devices due to the emission of volatile organic compounds (VOCs) and other chemicals from the breakdown of polyurethane foam used in these machines.

When the foam degrades, it can release harmful chemicals and toxic foam particles which users may inhale or ingest during device operation.

Many of these compounds may be potentially associated with various forms of cancer, including kidney cancer, due to their potential to cause cellular damage and disrupt normal cellular processes.

Prolonged exposure to these harmful chemicals is claimed to increase the risk of developing kidney cancer among users of these recalled devices.

Potential carcinogens identified from the degradation of the sound abatement foam include:

1. TDA (toluene diamine): TDA is a chemical that can be released during the breakdown of polyurethane foams; it is known for its use in the manufacture of polyurethane and other chemicals, potentially leading to respiratory issues and skin irritation when inhaled.
2. TDI (toluene diisocyanate): TDI is commonly used in the production of flexible polyurethane foams, which can off-gas from degrading foam in CPAP devices, causing severe respiratory problems and is a known carcinogen.
3. DEG (diethylene glycol): This compound may be emitted from breakdown products of foam adhesives and sealants used in manufacturing CPAP devices; DEG exposure is toxic to humans, potentially causing kidney and neurological damage.
4. DCM (dichloromethane): Often used as a solvent in the production of plastics and pharmaceuticals, DCM can be released from the breakdown of foam components in CPAP devices and is associated with cancer and central nervous system effects.

Philips Respironics Has Recalled Millions of Devices Due to Potential Health Risks

Philips Respironics initiated a massive CPAP recall in June 2021, effecting up to 15 million respiratory devices manufactured by the company.

The recall was prompted by the discovery that the polyester-based polyurethane (PE-PUR) foam used in these devices for noise abatement could degrade into particles that users might inhale or ingest.

Exposure to these particles and the volatile organic compounds they release has been linked to potential carcinogenic effects and other serious health issues.

Philips has acknowledged the risk and recommends that users of affected devices stop using them immediately and consult healthcare providers for alternatives.

The company has also committed to replacing or repairing the affected devices at no cost to users to mitigate the impact of the recall.

Philips faces hundreds of lawsuits from individuals claiming to have suffered health consequences due to prolonged exposure to the toxic chemicals released by the degrading foam.

What Philips Respironics Devices are Recalled?

Philips recalled several models of its CPAP machines, BiPAP machines, and Ventilator devices.

The recalled Philips CPAP machines, BiPAP machines, and Ventilator devices were distributed to consumers between 2009 and April 26, 2021.

Recalled Philips breathing machines include:

• A-Series BiPAP A30
• A-Series BiPAP A40 (ventilator)
• A-Series BiPAP Hybrid A30
• A-Series BiPAP V30 Auto (ventilator)
• C-Series ASV (ventilator)
• C-Series S/T and AVAPS
• DreamStation
• DreamStation ASV
• DreamStation Go
• DreamStation ST, AVAPS
• Dorma 400
• Dorma 500
• E30
• Garbin Plus, Aeris, LifeVent (ventilator)
• OmniLab Advanced+
• REMstar SE Auto
• SystemOne ASV4
• SystemOne (Q-Series)
• Trilogy 100 (ventilator)
• Trilogy 200 (ventilator)

Additionally, certain Trilogy Evo ventilators distributed from April 15, 2021, to May 24, 2021, with specific serial numbers were also recalled.

April 2024: Philips Respironics Hit With Consent Decree by the Federal Government

Philips Respironics has been issued a consent decree from a federal court following the significant recall of its sleep therapy machines, including CPAP and BiPAP devices.

The consent decree enforces a halt in the production and distribution of new devices from specific facilities until Philips meets rigorous safety and manufacturing standards set by the FDA.

The decree mandates Philips to execute a Recall Remediation Plan, ensuring affected patients receive either new devices, reworked devices, or partial refunds, reflecting the company’s responsibility to rectify the risks posed by their products.

Additionally, the decree includes stipulations for Philips to undergo regular inspections and adhere to strict regulatory compliances to prevent future violations.

Philips CPAP Lawsuit Overview

The Philips CPAP Lawsuit is related directly to the recall issued in June 2021, where millions of Philips CPAP, BiPAP, and ventilator devices were deemed unsafe due to potential health risks from degrading sound abatement foam.

Philips CPAP Machine Lawsuits have been consolidated into a multidistrict litigation (MDL), a process that centralizes pretrial activities for multiple lawsuits to improve efficiency, manage resources, and streamline the fact-finding process.

The Philips CPAP Recall MDL is designed to handle claims from thousands of individuals claiming that they have suffered serious health consequences as a direct result of using these defective devices.

These lawsuits generally claim that Philips was aware of risks associated with the polyester-based polyurethane (PE-PUR) foam used in their devices, which could degrade and emit harmful particles and gases, long before the recall was announced.

Plaintiffs argue that Philips failed to warn users about the potential for inhaling or ingesting toxic substances that could lead to cancer, respiratory issues, and other severe health problems.

Through these lawsuits, plaintiffs seek compensatory damages for medical costs, pain and suffering, lost wages, and other hardships they have endured due to the recalled CPAP devices.

CPAP Lawsuits aim to hold Philips accountable for alleged negligence in failing to ensure the safety and efficacy of their products before releasing them to the market.

The MDL and other legal proceedings intend not only to secure financial compensation for affected individuals but also to enforce stricter regulatory compliance and oversight to prevent similar public health issues in the future.

If you used a recalled Philips CPAP machine for sleep apnea and subsequently developed cancer, you may be eligible to file a Philips CPAP Lawsuit.

Contact TorHoerman Law for a free consultation.

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

What is the Philips CPAP Recall MDL?

The Philips CPAP Recall MDL refers to the multidistrict litigation established to manage lawsuits filed against Philips Respironics due to alleged harms caused by their recalled sleep apnea machines.

Unlike a class action, where plaintiffs are grouped into a single lawsuit under a representative party, an MDL consolidates multiple civil cases from different districts into a single district for pretrial proceedings, while maintaining each lawsuit’s individual claims and potential outcomes.

This process is particularly used to address complex cases involving many plaintiffs across various jurisdictions, like those involving the Philips CPAP machines, where issues of fact are common across cases but the specific damages or circumstances might differ.

The aim of the MDL is to streamline the discovery process, avoid conflicting rulings, and reduce the burden on the court system, while preserving the unique details and claims of each plaintiff’s case.

What is the Average Philips CPAP Lawsuit Settlement?

There has not yet been a global CPAP settlement reached in litigation against Philips Respironics.

However, lawyers estimate that average Philips CPAP settlement amounts may range from $50,000 to over $500,000.

These projections are by no means a guarantee of compensation in the Philips CPAP Lawsuit.

Philips CPAP Lawsuit settlement amounts are estimations based on prior mass tort lawsuits for defective medical devices.

It is essential that you contact a lawyer for a personalized and in-depth consultation to understand the circumstances of your case.

Reach out to our Philips CPAP Lawyers for a free consultation today, or use the chatbot on this page for an instant case evaluation.

Do You Qualify for the Philips CPAP Lawsuit?

Philips CPAP Recall Lawsuits filed against the medical device manufacturer are ongoing and have not been settled yet.

Lawyers are still investigating the case and speaking with individuals who used recalled Philips CPAP machines, BiPAP machines and ventilator devices and suffered related health problems.

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

Contact 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.

Experienced Philips CPAP Lawyers will help victims throughout the legal process, completing crucial steps such as gathering evidence and assessing damages.

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 claims, 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 kidney 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.