The Phillips Sleep Apnea Device Recall Includes Both Life-Supporting and Non-Life Supporting Models

Staying up to date with the latest information will help Phillips CPAP owners make informed decisions

Friday, September 17, 2021 - Former users of the recalled Phillips CPAP sleep apnea device and also the company's life-support ventilator products are encouraged to keep up with the latest developments. The company has set up a special website which they say will be updated every week and allow millions of former users to register their device and to receive replacement foam insulation and instructions on how to repair their machine. Each month the company will address a different defective model starting the other day with the Dream Station models. Royal Phillips, the maker of the CPAP devices admits that the foam that insulates and quiets the machine during the night while running causes toxic, carcinogenic particles, chemicals, and gasses to be released into the device's airways and directly into the user's lungs. Thousands of former users may have developed permanent lung damage the will lead to emphysema and lung cancer years down the road. Users should see a lung specialist immediately. Former users of Phillips CPAP machines should see their physician every year thereafter to have a better chance of catching the cancer early and successfully treating the disease. If you or a loved one have been using a model of the Phillips CPAP machine that has been recalled, and received a diagnosis of lung cancer, you should speak with a Phillips recall lawyer to see if you qualify to file a Phillips CPAP cancer lawsuit.

The Food and Drug Administration (FDA) is lending guidance to former CPAP users and publishing every week on the internet. To summarize, the FDA issued a total recall of Phillips CPAP devices on June 30, 2021, saying "The U.S. Food and Drug Administration (FDA) is alerting people who use Philips Respironics ventilators, BiPAP, and CPAP machines and their health care providers that Philips Respironics has recalled certain devices (see table below) due to potential health risks." Phillips devices fall into one of two categories, life-supporting or non-life-supporting. Most sleep apnea CPAP users fall into the non-life supporting category. According to the FDA website, the non-life supporting Phillips devices covered by the recall are DreamStation ASV, DreamStation ST AVAPS, SystemOne ASV4, C-Series ASV, C, Series S/T and AVAPS, and the OmniLab Advanced Plus. Owners of one of these devices that have not complied with the recall should contact the company's website for specific instructions. The company website advises that a life support ventilator should continue to be used, and the risks of discontinuing usage weighed against the benefits the machine provides to seriously ill patients. The models of Phillips life-support machines included in the recall are the Trilogy 100, Trilogy 200, the Garbin Plus, Aeris, and the LifeVent models. The FDA urges both types of users to consult with a physician before discontinuing and consider their health profile. Should your device fall into the category of non-life support, the FDA tells readers to consider alternative sleep apnea solutions. "Using alternative treatments for sleep apnea, such as positional therapy or oral appliances, which fit like a sports mouthguard or an orthodontic retainer," The FDA writes.

More Recent Philips CPAP Cancer Lawsuit News:

• Results of Phillips-Funded Studies Call The Use of Ozone Cleaning Products Into Question | 7/20/2022
• Phillips CPAP Malfunctions And Using An Ozone Cleaning Solution May Go Hand In Hand | 7/10/2022
• SoClean Cleaning Solution Is Accused Of Being Unsafe And May Have Contributed To Phillips CPAP Malfunction | 7/2/2022
• Bloomberg Alleges Phillips Knew Of The Health Hazards From Sound Abatement Foam Years Before The CPAP Recall | 6/14/2022
• The FDA Is Recalling 55,000 Ventilators Made By Phillips Respironica | 6/7/2022
• Phillips Respironics Sleep Apnea Machine Recall Falls Far Short Of Expectations | 6/3/2022
• People Are Dying From Cancer And Suing Phillips Respironics For Negligence Leading To Personal Injury | 5/24/2022
• A Wrongful Death Lawsuit Claims The Foam Manufacturer Is Liable For Using Substandard Material | 5/9/2022
• A Wrongful Death Lawsuit Claims The Foam Manufacturer Is Liable For Using Substandard Material | 5/9/2022
• Sleep Apnea Patients From The Cleveland Clinic Want To Know When To Expect Their DreamStation Sleep Apnea Machine Replacement | 4/28/2022
• Unapproved Ozone Cleaning Contraptions May Be A More Likely Cause of CPAP Airway Contamination | 4/20/2022
• Phillips CPAP Lawsuits Allege The Machine Causes Varying Degrees of Respiratory Illnesses | 4/5/2022
• Medical Device Suppliers Are Filing Phillips CPAP Sleep Apnea Lawsuits | 3/29/2022
• The US Food And Drug Administration Considers The Phillips CPAP Recall Efforts To Be Ineffective | 3/18/2022
• Phillips Respironics May Not Have A Suitable Solution To Their Defective Sleep Apnea Devices | 2/25/2022
• Phillips Telling Patients To Consult With Their Physicians Before Discontinuing Using The Recalled Sleep Apnea Device | 2/21/2022
• US Government Regulators Acknowledge The Serious Nature Of The Phillips CPAP Cancer Recall With Class 1 Recall | 2/11/2022
• Phillips Respironics And SoClean Inc. May Have To Share Responsibility For CPAP User Cancer | 2/7/2022
• Phillips Respironics Waited Too Recall Sleep Apnea Machines And Their Customers Died As A Result | 2/2/2022
• The FDA Thinks The Phillips CPAP Machines May Lead To Developing Deadly Forms of Cancer | 1/28/2022
• The FDA Tells CPAP Users That SoClean Ozone Cleaning Solutions Are Not Legally Marketed | 1/14/2022
• Sleep Apnea May Affect Millions More Than Those Using CPAP Devices | 1/10/2022
• Phillips Delayed The CPAP Recall Until Another Device Could Be Sold To Consumers | 1/4/2022
• FDA Accusations Of A Coverup Will Be Hard For Phillips To Dismiss | 12/29/2021
• A Women Allegedly Developed Breast Cancer From Using The Phillips CPAP Sleep Apnea Machine | 12/22/2021
• Phillips And SoClean May Be Forced To Share Legal Responsibility For Failing To Warn Consumers | 12/16/2021
• Royal Phillips Versus SoClean Inc. Could Determine The Outcome Of DreamStation CPAP Lawsuits | 12/1/2021
• Recalled Phillips Sleep Apnea Devices Could Approach 15 Million Units Or More | 11/24/2021
• Sleep Apnea Patients Look To Replace Their Recalled Phillips CPAP Machine Since Phillips Seems Incapable | 11/17/2021
• Ozone Cleaning Products Are Not FDA Approved And May Be Responsible For CPAP Foam Insulation Breakdown | 11/12/2021
• CPAP Plaintiffs Suffer Anxiety From Not Knowing How Severe Their Lung Problems May Be | 11/8/2021
• New Lawsuits Allege CPAP User Developed Pancreatic Cancer From Using the DreamStation CPAP device | 11/1/2021
• Sleep Apnea Patients Continue To Use Their CPAP Device Because They Are Unable To Function The Next Day Without It | 10/27/2021
• Problems Mount For Royal Phillips From Multiple Sources Over CPAP Machine Malfunctions | 10/23/2021
• Royal Phillips Battles SoClean For Responsibility In Causing Lung Disease And Disorders | 10/19/2021
• Phillips NV Claims That A Third-Party Cleaning Solution Is The Cause Of Their Sound Abatement Foam Degrading | 10/14/2021
• The US Attorney General Is Concerned Phillips Is Failing To Deliver a Timely CPAP Solution | 10/11/2021
• A Sleep Apnea Doctor Offers Sound Advice For Patients In The Wake Of The Phillips CPAP Recall | 10/5/2021
• Sleep Apnea Problems Continue For Millions Affected By The CPAP recall | 9/29/2021
• Phillips DreamStation CPAP Turns Into a Nightmare For Millions of Users | 9/27/2021
• Phillips CPAP DreamStation Cancer Could Go Undetected For A Decade | 9/23/2021
• Phillips CPAP Stockholders Were Tipped Off About CPAP Failures More Than A Month Before Millions of Users | 9/14/2021
• The Phillips Sleep Apnea Machine Recall And Replace Affects Mostly US Owners | 9/9/2021
• Phillips CPAP Sleep Apnea Device Recall Will Begin Soon But Could Take One Year To Complete | 9/6/2021
• Phillips CPAP Users May Have A Replacement Device Coming Within The Next Several Months | 9/1/2021
• FDA Recall Classification of Phillips CPAP Devices Is The One Reserved For The Most Worrisome Medical Devices | 8/26/2021
• Charities Re-Purpose Non-Essential Sleep Apnea Machines Into Covid-19 Ventilators | 8/24/2021
• The Life or Death Demand Created By The Delta Variant Of Covid-19 Magnifies The Need For Safe Ventilators | 8/20/2021
• Former Phillips CPAP Users May Not Get A Replacement For Months | 8/18/2021
• You May Have Sleep Apnea And Not Know It | 8/16/2021
• Lawsuits Are Being Filed By People That Have Developed Cancer From Using The Phillips Sleep Apnea Device | 8/11/2021

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.