Philips Respironics recently recalled several models of Continuous Positive Airway Pressure (CPAP) and Bilevel Positive Airway Pressure (BiPAP) machines. These machines help individuals with sleep apnea regulate their breathing while they sleep.
These machines were recalled because of a defect that could expose users to toxic gases and potential carcinogens. Individuals across several states have brought lawsuits asserting that the design of the machines was faulty and posed an unreasonable risk of harm to the people who used them.
If you have symptoms or a cancer diagnosis that you believe might be related to using one of the recalled Philips machines, a local mass torts attorney could help you seek compensation from liable parties. If you qualify, Buda CPAP lawsuits might provide a means for you to get the restitution you deserve.
These specific products are being investigated for mass tort claims:
- E30 (Emergency Use Authorization)
- DreamStation ASV
- DreamStation ST, AVAPS
- SystemOne ASV4
- C Series ASV, S/T, AVAPS
- OmniLab Advanced Plus In-Lab Titration Device
- SystemOne (Q series)
- DreamStation CPAP, Auto CPAP, BiPAP
- DreamStation GO CPAP, APAP
- Dorma 400, 500 CPAP
- REMStar SE Auto CPAP
- Trilogy 100 Ventilator
- Trilogy 200 Ventilator
- Garbin Plus, Aeris, LifeVent Ventilator
- A-Series BiPAP V30 Auto Ventilator
If you or a loved one has used one of these and later suffered from any of the following illnesses or side effects, consider contacting a lawyer for further investigation:
- Respiratory Failure
- Pulmonary Fibrosis
- Idiopathic Pulmonary Fibrosis
- Autoimmune Disorders
- Chronic Asthma
- Interstitial Lung Disease
- Chronic Bronchitis
- Acute Inhalation Injury
- Heart Failure
- Kidney Disease
- Liver Disease
Hazardous Insulating Foam in CPAP Machines
The recalled CPAP and BiPAP machines contained polyester-based polyurethane (PE-PUR) insulating foam to reduce vibration and suppress noise. However, the company has received reports that the foam disintegrates and forms into small pieces of black debris that migrate to the machine’s air pathways, causing a user to inhale or ingest these particles. The foam also emits gases that might be toxic.
The Food and Drug Administration (FDA) determined that using a CPAP machine with degraded PE-PUR foam could pose a significant threat of health complications or death. Because of the significance risk to someone’s health, the FDA issued a Class I recall – its most urgent recall action.
Some of the health complications that have been linked to ingesting or inhaling the degraded foam, or breathing the toxic off-gases, include:
- Skin and eye irritation
- Upper respiratory system symptoms
- Carcinogenic effects
Anyone in Buda who developed symptoms related to degraded PE-PUR exposure or received a diagnosis of cancer in the kidney, liver, colon, or lungs after using a Philips CPAP or BiPAP machine should speak with an attorney right away about filing a lawsuit.
Strength and Efficacy in Numbers
When there are multiple plaintiffs suffering the same harm from a single product or group of products, a mass torts lawsuit could be the best way to proceed. A mass tort action is a lawsuit with multiple plaintiffs alleging common losses against a defendant or group of defendants. In this case, the defendant would be Philips Respironics.
An experienced attorney in the Buda area could advise an injured or sick individual on how to best proceed with mass tort litigation for harms suffered as a result of a defective CPAP or BiPAP machine. Do not face the legal process without skilled representation from a local lawyer.
Consult with a Buda Attorney about Your CPAP Lawsuit
If you used one of the recalled Philips machines and you have developed cancer or other severe symptoms, contact a local lawyer right away. You could join one of the Buda CPAP lawsuits and get compensation for the harm that the defective machine caused you.
There is a window of opportunity to take effective action now. Take advantage by calling a seasoned lawyer about your CPAP case today.