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Philips CPAP Lawsuit

Philips CPAP Recall List

Philips, a manufacturer of popular CPAP, BiPAP, and ventilators, has recalled millions of its defective machines, which contain a toxic polyester-based foam that also contains a known carcinogen. 

Recalled Philips device brands include:

  • Aeris

  • BiPAP A30/A40 Series Device Models

  • BiPAP V30

  • C-Series ASV

  • Dorma 400 and 500

  • DreamStation

  • E30

  • Garbin Plus

  • LifeVent

  • REMstar SE Auto

  • SystemOne (Q-Series)

  • Trilogy 100

  • Trilogy 200

Medical Issues Caused by Recalled Philips CPAP Devices

Use of them may cause lung and respiratory problems and other temporary and potential permanent physical injuries (headaches, respiratory irritation, chest pressure, cough, sinus infections), and even cancers, including:

  • Acute Respiratory Distress System (ARDS)

  • Bladder Cancer

  • Brain Cancer

  • Breast Cancer

  • Chemical Poisoning

  • Heart Attack

  • Heart Failure

  • Hematopoietic Cancer

  • Kidney Cancer

  • Kidney/Renal Damage

  • Kidney/Renal Disease

  • Leukemia

  • Liver Cancer

  • Liver Damage

  • Liver Disease

  • Lung Cancer

  • Lung Damage

  • Lung Disease

  • Lymphatic Cancer

  • Multiple Myeloma

  • Nasal Cancer

  • Non-Hodgkin Lymphoma

  • Papillary Carcinoma

  • Pleural Effusion

  • Prostate Cancer

  • Reactive Airway Disease (RAD)

  • Rectal Cancer

  • Respiratory Failure

  • Severe Ear Inflammation

  • Severe Nose Inflammation

  • Severe Throat Inflammation

  • Stomach Cancer

  • Testicular Cancer

  • Thyroid Cancer

Individuals who have used these products may have a claim.

Contact a Philips CPAP lawsuit lawyer at Petway, French & Ford today to find out more.

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