Philips CPAP Cancer Lawsuit News

The FDA Is Recalling 55,000 Ventilators Made By Phillips Respironica

The Phillips V60 ventilators join their complete line of sleep apnea machines as those being recalled because they can cause permanent health damage or death

Tuesday, June 7, 2022 - According to the US Food and Drug Administration (FDA), another massive recall of Phillips sleep apnea machines and ventilators is underway. Phillips Respironics has been forced to recall all V60 and V60 Plus ventilators because they may suddenly stop working due to internal power fluctuations. The shutdown may or may not trigger the alarm. The FDA reported the issue to be a faulty power supply. The recall is that of Type I, an FDA designation reserved for drugs or medical devices that may cause personal injury or death if they malfunction when used as directed. The two ventilators in question are used by adults and children who can breathe on their own but need help and are under hospital care. "with respiratory failure, chronic respiratory insufficiency, or obstructive sleep apnea.” The ventilators are used in hospitals or other institutional settings under the direction of health care professionals," according to the FDA. The FDA warns that the Phillips ventilator shut down could deprive a person of oxygen for an extended time causing adverse health consequences and death. "As of April 14, 2022, there have been reports of 4 injuries and 1 death associated with the use of the recalled devices," the FDA tells readers. About 55,000 ventilators are subject to the recall and users should register their devices online to receive a replacement. Other medical devices made by Phillips Respironics, a Dutch company, have a history of malfunctioning with catastrophic health consequences. Phillips has issued a recall of more than 3 million of its sleep apnea relief machines. Phillips Respironics is being sued by hundreds of sleep apnea patients after their prescribed sleep apnea device leached toxic particles, chemicals, and gasses into the device's airway, leading allegedly to developing Phillips CPAP cancer and other serious, irreversible respiratory illnesses. CPAP cancer lawsuits allege that the device's sound abatement foam degrades causing carcinogens to be released. If you or a loved one have been using a Phillips ventilator that stopped working and caused injury or death you are urged to contact a Phillips CPAP lawyer to see if you qualify to file a claim against the manufacturer.

Phillips Respironics recommends that hospitals continue to use the ventilators in question but to make sure they are hooked up to a nurse/call backup remote call system should the initial warning fail to alert medical staff and to verify the backup alarm system works before using the device. Phillips also recommends hospitals and individuals have a backup ventilator ready to be used. The US Department of Justice has formally warned Phillips to immediately comply with the FDA's CPAP recall. The company is accused by its customers of dragging their feet and not sending them a replacement device. Sleep apnea is a serious medical condition that can lead to developing heart disease or diabetes if not treated properly. Many Phillips sleep apnea customers are still unaware of the device's mechanical breakdown.

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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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