Philips CPAP Cancer Lawsuit News

FDA Recall Classification of Phillips CPAP Devices Is The One Reserved For The Most Worrisome Medical Devices

The FDA has identified the Phillips CPAP recall as a Class I recall, the most serious type reserved for devices that may cause serious injuries or death

Thursday, August 26, 2021 - Thousands of Phillips CPAP lawsuits have been filed against Royal Phillips, a corporation based in the Netherlands, and the maker of several different sleep apnea and ventilator devices, for failing to warn their customers that the device could leach deadly toxins directly into a person's airways leading to lung disease and lung cancer. The Food and Drug Administration (FDA) sent out a warning a couple of months ago and recalled the Philips BiPAP / CPAP units labeled the CPAP (continuous positive airway pressure) machines and BiPAP (bilateral positive airway pressure) machines, calling their malfunctions life-threatening. These products were to relieve sleep apnea and also provide life-support for people suffering from Covid-19. Instead the device produces toxic particles and chemicals into the device's and the user's airways and lungs. The Phillips.com sleep apnea machine website tells patients, "On June 14, 2021, Philips issued a recall notification for the United States for specific affected ventilation and sleep apnea devices. Stop use of BiLevel PAP & CPAP sleep apnea devices."

People that suffer from sleep apnea wake up many times during the night from the sound of their snoring. Many sleep apnea patients stop breathing and wake up gasping for air. Most sleep apnea patients fail to recognize their problem, and it is up to a sleeping partner to identify the condition by its symptoms. Millions of Americans were using the defective Phillips CPAP machines when advised to stop and wait for further recall instructions. As of today, no one knows when replacement machines will be made available, if at all, leaving former Phillips CPAP clients confused, scared, and in need of answers that are not forthcoming. Hospitals that have had their Phillips ventilators recalled may not be complying with the FDA since the risks of stopping using the machine may outweigh the detrimental health effects that the product's malfunction has caused. Doctors have the responsibility to assess each Covid-19 patient individually and consider the gravity of the illness. Some hospitals have constructed workarounds and added filters to try and sanitize the air going into their patient's lungs.

If you or a loved one have developed lung disease or lung cancer from using one of the Phillips CPAP devices, you may wish to speak with a Phillips CPAP recall lawyer to see if you qualify to file a claim. Patients, users, and caregivers should contact Phillips directly to begin the registration process that could lead to receiving a replacement machine or instructions on making the necessary repairs. Patients using mechanical ventilators should continue life-sustaining ventilation therapy such as treatment for the respiratory symptoms of Covid-19. With a lack of information from the company, sleep apnea patients should see a lung specialist and ascertain the degree of lung damage the device has caused.

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Lawyers for CPAP Cancer Lawsuits

We will represent all persons in involved in a BiPAP or CPAP cancer lawsuit on a contingency basis, meaning there are never any legal fees unless we win compensation in your case. Anyone who developed cancer or another serious side effect as a result of using a Philips CPAP sleep apnea machine or ventilator in --or is a family member of such a person--is eligible to receive a free, no-obligation case review from our attorneys. Simply contact our firm through the online contact form or the chat feature and one of our Philips BiPAP cancer lawyers serving will contact you promptly to discuss your case.



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