Philips CPAP Users Left to Pay Out of Pocket or Risk Serious Injury, Cancer After June 2021 Recall

A potentially dangerous defect resulted in millions of continuous positive airway pressure (CPAP machines) to be recalled in June 2021.

While Philips Respironics, the company who manufactures these CPAP machines, is offering to fix or replace these machines, the wait times have been extended into September 2022. That is a long time for users who rely on these machines to survive to wait. The only other option is to purchase a machine out of pocket from another manufacturer.

Here is a list of the recalled devices:

  • E30 (Emergency Use Authorization)
  • DreamStation ASV
  • DreamStation (ST, AVAPS)
  • SystemOne (ASV4)
  • C Series (ASV, S/T, AVAPS)
  • OmniLab Advanced Plus (In-Lab Titration Device)
  • SystemOne (Q Series)
  • DreamStation (CPAP, Auto CPAP, BiPAP)
  • DreamStation GO (CPAP, APAP)
  • Dorma 400,500 (CPAP)
  • REMStar SE Auto (CPAP)
  • Trilogy100
  • Trilogy 200
  • A-Series BiPAP Hybrid (A30) – not marketed in the United States
  • A-Series BiPAP V30 (Auto)
  • Garbin Plus, Aeris, LifeVent
  • A-Series BiPAP A40
  • A-Series BiPAP A30

If you or a loved one are in need of a repair or replacement for a Philips CPAP machine, you can apply here.

Side Effects of Using a Defective Philips CPAP Machine

Recalled devices

Philips CPAP machines were recalled following complaints that these machines were releasing degraded foam particles and chemical emissions for users to inhale or ingest. The possible symptoms associated with degraded foam exposure include:

  • Irritation or inflammation to the upper airway
  • Cancer
  • Asthma
  • Sinus infections
  • Headaches
  • Kidney, liver, or other organs failing
  • Irritation to the respiratory tract
  • Pressure in chest
  • Chronic cough

Exposure to chemical emissions from Philips CPAP machines can lead to:

  • Headaches
  • Irritation to the respiratory tract
  • Dizziness
  • Nausea or vomiting
  • Hypersensitivity

Recover Compensation Through a Philips CPAP Defective Machine Lawsuit

If you suffered harm after using a recalled sleep apnea machine, then you may be eligible to recover financial damages for your losses. These can include all past, present and future medical costs, a replacement CPAP machine, lost wages, pain and suffering, and other economic losses related to your injuries.

Our Citrus County Phillips CPAP Device Recall Lawyers at Whittel & Melton can review the details of your claim and provide you with a better understanding of the financial compensation that may be available to you.

Class Action Lawsuits Against Philips Exploding in 2022

Class action lawsuits against Philips are anticipated to boom in 2022. If you have been using one of the recalled Philips CPAP machines listed above and would like more information on how you can join the CPAP class action lawsuit, then we urge you to contact our Citrus County Phillips CPAP Device Recall Lawyers at Whittel & Melton today at 352-726-0078 or contact us online. We are now taking on new cases stemming from defective Philips CPAP breathing machines. We want to help you fight for the compensation you need and deserve after using a dangerous and defective device. Contact us now so that we can offer you a free case review and discuss your legal rights and options.

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