Philips CPAP Recall
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Philips CPAP Recall Lawsuit Attorneys
We’re Advocating for Those Injured Nationwide
The U.S. Food and Drug Administration (FDA) issued a recall on various Philips CPAP, BiPAP, and ventilators after reports of respiratory problems and lung cancer, among other injuries. While the CPAP recall will prevent future injuries, it is too late for the many Americans already injured by these machines. No one should be put in harm’s way by a medical device they were told could improve their health and help them manage their symptoms.
Has a Philips Respironics CPAP machine caused you or a loved one injury? If so, Houssiere Durant & Houssiere, LLP is here to advocate for you. Our Houston trial lawyers are reviewing cases nationwide involving defective Philips Respironics sleep apnea machines. Those injured may have grounds to file suit against Philips for financial compensation.
If you have been injured, find out if you qualify to file a Philips CPAP recall lawsuit. Call (888) 881-8100 today for a free consultation with a national lawyer.
Potential Health Risks and Injuries
After receiving numerous complaints of injury, the FDA investigated Philips Respironics CPAP, BiPAP and Ventilators machines for potential health hazards. It found that the polyester-based polyurethane (PE-PUR) sound abatement foam in these machines, which reduces sound and vibration, is likely to deteriorate and enter the machine’s air pathway. This puts the user at risk of accidentally swallowing the foam’s black debris and/or inhaling carcinogenic chemicals. So, what are the Philips CPAP recall symptoms and health risks? Our defective products attorneys have gathered the following list.
The potential health risks associated with recalled Philips sleep apnea machines include but are not limited to:
- Lung, liver, and blood cancer
- Asthma
- Confusion
- Headaches
- Hypersensitivity
- Dizziness and fainting
- Nausea and vomiting
- Eye, skin, nose, and throat irritation
- Liver disease
- Kidney disease
Philips Respironics Sleep Apnea Machines Under Recall
The investigation spurred the FDA to implement a Class I recall, the most serious type of recall, on the following CPAP and BiPAP machines manufactured between 2009 and April 26, 2021:
- Continuous Ventilator, Minimum Ventilatory Support, Facility Use
- E30 (Emergency Use Authorization)
- Continuous Ventilators, Non-Life Supporting
- DreamStation ASV
- DreamStation ST, AVAPS
- SystemOne ASV4
- C-Series ASV
- C-Series S/T and AVAPS
- OmniLab Advanced+
- Noncontinuous Ventilators
- SystemOne (Q-Series)
- DreamStation
- DreamStation Go
- Dorma 400
- Dorma 500
- REMstar SE Auto
The below Philips ventilators manufactured during the same period have also been recalled:
- Continuous Ventilators
- Trilogy 100
- Trilogy 200
- Garbin Plus, Aeris, LifeVent
- Continuous Ventilators, Minimum Ventilatory Support, Facility Use
- A-Series BiPAP Hybrid A30
- A-Series BiPAP V30 Auto
- Continuous Ventilators, Non-Life Supporting
- A-Series BiPAP A40
- A-Series BiPAP A30
Potential Compensation You Could Recover
If your Philips CPAP recall lawsuit is successful, you may be entitled to recover compensation for the losses, or damages, you have experienced. Common damages include lost wages, pain and suffering, and the cost of medical care, such as hospital bills, rehabilitative treatments, and medications.
Put Our Technical Knowledge to Work for You
Our firm’s senior partner, Charles “Chip” Houssiere, is uniquely qualified to help clients with claims involving defective Philips CPAP machines. Medical devices are designed and manufactured with both medicine and engineering in mind. In his past work with NASA, Chip studied how the conditions of outer space would affect an astronaut’s cardiovascular system. He is, therefore, well educated in the concepts and language medical device makers use in their lawsuits. He can effectively argue your case in court, as he is fluent in the language of medical science.
Get Started with Your Philips CPAP Recall Lawsuit Today
With 40 years of experience, Houssiere Durant & Houssiere, LLP’s attorneys are prepared to represent you in your Philips Respironics recall case. Although Philips has now recalled these defective machines, we will not let it get away with pushing them to market in the first place. We fully intend to use our technical and legal skills to secure your full compensation. Work with a compassionate, honest, and relentless team of trial attorneys who will make you a priority.
Contact Houssiere Durant & Houssiere, LLP online to get in touch with a national lawyer. Your consultation is free.
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Join The Phillips CPAP Recall Lawsuit
Philips Respironics Sleep Apnea Machines Under Recall
The investigation spurred the FDA to implement a Class I recall, the most serious type of recall, on the following CPAP and BiPAP machines manufactured between 2009 and April 26, 2021:
- Continuous Ventilator, Minimum Ventilatory Support, Facility Use
- E30 (Emergency Use Authorization)
- Continuous Ventilators, Non-Life Supporting
- DreamStation ASV
- DreamStation ST, AVAPS
- SystemOne ASV4
- C-Series ASV
- C-Series S/T and AVAPS
- OmniLab Advanced+
- Noncontinuous Ventilators
- SystemOne (Q-Series)
- DreamStation
- DreamStation Go
- Dorma 400
- Dorma 500
- REMstar SE Auto
The below Philips ventilators manufactured during the same period have also been recalled:
- Continuous Ventilators
- Trilogy 100
- Trilogy 200
- Garbin Plus, Aeris, LifeVent
- Continuous Ventilators, Minimum Ventilatory Support, Facility Use
- A-Series BiPAP Hybrid A30
- A-Series BiPAP V30 Auto
- Continuous Ventilators, Non-Life Supporting
- A-Series BiPAP A40
- A-Series BiPAP A30
Potential Compensation You Could Recover
If your Philips CPAP recall lawsuit is successful, you may be entitled to recover compensation for the losses, or damages, you have experienced. Common damages include lost wages, pain and suffering, and the cost of medical care, such as hospital bills, rehabilitative treatments, and medications.
Put Our Technical Knowledge to Work for You
Our firm’s senior partner, Charles “Chip” Houssiere, is uniquely qualified to help clients with claims involving defective Philips CPAP machines. Medical devices are designed and manufactured with both medicine and engineering in mind. In his past work with NASA, Chip studied how the conditions of outer space would affect an astronaut’s cardiovascular system. He is, therefore, well educated in the concepts and language medical device makers use in their lawsuits. He can effectively argue your case in court, as he is fluent in the language of medical science.
Get Started with Your Philips CPAP Recall Lawsuit Today
With 40 years of experience, Houssiere Durant & Houssiere, LLP’s attorneys are prepared to represent you in your case. Although Philips has now recalled these defective machines, we will not let it get away with pushing them to market in the first place. We fully intend to use our technical and legal skills to secure your full compensation. Work with a compassionate, honest, and relentless team of trial attorneys who will make you a priority.
Contact Houssiere Durant & Houssiere, LLP online to get in touch with a national lawyer. Your consultation is free.
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