Recalled Phillips Sleep Apnea Devices Could Approach 15 Million Units Or More
In 2015, Phillips failed to investigate reports one of their units were repairing foam degradation of Trilogy Ventilators
Wednesday, November 24, 2021 - The results of a recent FDA investigation into the Phillips CPAP sleep apnea devices recall has concluded that the number of machines under recall is much higher than we were told at first by the manufacturer. AboutLawsuits.com (AL) tells readers that FDA inspection reports that the 3 million-unit Phillips CPAP recall in the summer of 2021 fell far short of the 15 million units that were defective and were injuring users. People who have developed cancer or another serious respiratory illness as a result of using a Philips CPAP breathing machine or mechanical ventilator may be eligible for lump-sum monetary compensation by filing a Philips CPAP cancer lawsuit. The report also suggests that Phillips was non-responsive when the first reports of the machine's problems were made to them years ago. "While initial media reports suggested that Philips Respironics was recalling about 3 million DreamStation, CPAP, BiPAP, and mechanical ventilators in June 2021, the FDA inspection report (PDF) issued late last week indicates that over 15 million devices have been recalled, and that may not include all CPAP machines that pose a health risk for consumers," according to AL.
Phillips defends their actions by citing that the Phillips CPAP recalls are ongoing and have no formal start or stop date. The FDA tells consumers that the Trilogy ventilator devices should have also been included in the company's Class I recall years ago when complaints were made but were not. The report goes on to say that Phillips should have been aware of the Trilogy device's noise abatement foam deterioration problem as early as November 11, 2015, when other units within the company were making such repairs. The FDA has accused Phillips of failing to take action after the company became aware that another unit of the company had performed service on the noise abatement foam used on the Trilogy model and took no further actions. The FDA or around 11/25/15, your firm was aware and knowledgable of a preventative maintenance servicing procedure implemented by another Phillips entity on Trilogy ventilator products, and no further investigation, health hazard evaluation, risk analysis, or design review was performed, or documented by your firm. The preventative maintenance was implemented by Phillips LTD, (the other entity) only, and in response to foam degradation issues and complaints in the field related to Trilogy ventilator products." The FDA report lays bare that Phillips continued to market their sleep apnea machines and even highlighted their quiet operation because of the PE-PUR noise abatement foam that the company either knew or had an obligation to know was degrading and releasing toxic, carcinogenic particles, chemicals and gassed directly into the machine's airway to be inhaled by the user.
Failing to immediately investigate reports of foam degradation reflects poorly on the company and is in line with the lack of effort the company has put into recalling and replacing the 3 million Phillips CPAP units under the current recall. In October, Attorney General William Tong instructed the Food and Drug Administration (FDA) to increase its supervision efforts and pressure Royal Phillips to speed up the repair and replacement of millions of Phillips Sleep Apnea devices.
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
- 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
- The Phillips Sleep Apnea Device Recall Includes Both Life-Supporting and Non-Life Supporting Models | 9/17/2021
- 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.