Philips Recalls Millions of CPAP, BiLevel PAP, & Ventilator Machines Over Health Risks
Philips, a medical device manufacturer, is recalling several sleep apnea machines and ventilators due to a potential cancer risk and other health issues. This recall impacts an estimated 3 to 4 million devices globally. A majority of these are devices intended to assist individuals with sleep apnea, while the remainder are mechanical ventilators.
The concern centers around a polyester-based polyurethane sound abatement foam used in these machines, which, if broken down, can release harmful particles and toxic gases. These emissions could potentially lead to health complications including irritation, nausea, headache, inflammation, vomiting, and even cancer.
Injuries Named in CPAP Lawsuits
Deteriorating noise reduction foam in Philips' CPAP machines has been linked to various health issues, prompting legal action alleging the devices contribute to cancer and damage to organs. Philips acknowledged receiving user complaints about symptoms such as headaches, difficulty breathing, chest discomfort, coughing, and sinus infections. Additionally, there's concern about more severe hazards, potentially leading to life-threatening conditions or lasting harm.
Lawyers Are Accepting Philips CPAP Lawsuit Claims From People Who Suffered the Following Injuries After Using One of the Recalled Devices: