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Millions of DreamStation devices were recalled because sound abatement foam can degrade into toxic particles. If you inhaled these particles and got sick, you may be entitled to compensation.
*Personal injury claims are still being evaluated for individual payouts.
Philips used a polyester-based polyurethane (PE-PUR) foam to reduce sound and vibration in their ventilators and CPAP machines.
It was discovered that this foam breaks down over time, especially in high heat or humid conditions, or when cleaned with ozone cleaners. Users were unknowingly inhaling black debris and toxic VOC gases directly into their lungs while they slept, causing severe respiratory issues and cancer.
Direct inhalation of carcinogens.
Scarring of lung tissue.
Toxic chemicals entering bloodstream.
Severe asthma, COPD exacerbation.
Note: The recall affects devices manufactured between 2009 and April 2021.
Following the recent $1.1 billion settlement for personal injury claims, payouts are being categorized by injury severity.
New onset Asthma, COPD worsening, or Chronic Bronchitis without hospitalization.
Pulmonary Fibrosis, Sarcoidosis, or Cancer requiring surgery/treatment.
Advanced Lung Cancer, Head/Neck Cancer, or Wrongful Death.
Updates on MDL 3014 settlements and recalls.
Settlement ReachedPhilips has agreed to pay over $1 billion to settle personal injury and wrongful death claims in the US. The settlement does not include an admission of liability.
Read Article →
Recall InfoThe FDA has issued new warnings regarding the safety of refurbished DreamStation devices, citing potential overheating and thermal issues.
Read Article →
Medical DataNew independent lab tests suggest the degraded foam particles may cause DNA damage, strengthening the link to cancer development.
Read Article →If you used a recalled Philips device and developed cancer or respiratory issues, act now before the claim deadline passes.
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