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The victims who have suffered serious injuries and medical conditions from recalled Phillips® brand CPAP & BIPAP devices are requested to finally seek justice beginning with a free, private case evaluation

The victims who have suffered serious injuries and medical conditions from recalled Phillips® brand CPAP & BIPAP devices are requested to finally seek justice beginning with a free, private case evaluation

Those patients who’ve suffered may be eligible for significant compensation, as these recalled devices have been linked to:

  • prostate cancer
  • sinus cancer
  • throat cancer
  • kidney & liver cancer
  • leukemia & multiple myeloma
  • lung disease/asthma/sarcoidosis
  • kidney/liver damage & disease
  • pneumonia
  • breast cancer
  • other cancers & more...

Limited Time To File A Claim. Check Eligibility Today.

Important Update

The FDA just dropped an update on that Philips sleep apnea machine recall, and it's quite an eye-opener. They're saying these machines might be connected to a whopping 561 reported deaths.

Since April 2021, the FDA has been flooded with over 116,000 reports about these respiratory devices. They've been breaking down and causing some serious health risks. This includes talking, choking, inhaling weird particles, and even an increased chance of cancer.

These devices, used for sleep apnea and similar disorders, were made with a foam called polyester-based polyurethane (PE-PUR). However, this foam breaks down over time, and the little bits can end up in the airways of the people using them. The FDA warns you might end up breathing in these "black pieces of foam" or some invisible chemicals.

After the first recall of over 5 million devices in 2021, Philips tried to sort out the issue. But they still fail to meet safety standards or consumer expectations.

Philips has now agreed to stop selling these devices in the U.S., primarily because of the filing of a proposed class action settlement.

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Phillips® CPAP and Ventilation Machines are Causing Damage That is Being Reported

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Philips Respironics® recalled millions of CPAP and BiPAP machines because degraded PE-PUR sound abatement foam in the machines may break down and cause serious health issues, including:

  • Cancer
  • Respiratory inflammation and
  • Other toxic effects

The Philips® CPAP recall includes the Philips Dreamstation and other popular CPAP machines.

Phillips® has announced that they’re recalling between 3 and 4 million CPAP and ventilation devices due to disintegrating sound-reducing foam.

Consumers have begun to report suffering serious side effects that include kidney/liver damage, wide ranging chemical poisonings, and other unhealthy conditions.

Many consumers experience serious and long-lasting side effects from the chemical from the recalled machines, including cancers, strokes, and a variety of cancers.

Consumers that have used particular Phillips® CPAP and ventilation machines and suffered any of these symptoms should come forward to file claims for compensation — legal case evaluations are free of charge and private.

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Which Philips© CPAP Ventilators and Machines Have Been Recalled?

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With a surge in the number of Philips© CPAP ventilators and machines linked to respiratory issues, chemical poisonings, and much more, recalls on these pieces of medical equipment are more frequent, as well.

The recall doesn’t affect all of Philips®’ breathing devices.

About 80% of the affected devices are CPAP machines and about 20% are ventilators, Philips® spokesman Steve Klink told Reuters.

Most of the devices come from Philips’ DreamStation® line.

The recall affects all serial numbers of the following affected devices manufactured between 2009 and April 26, 2021.

More than half of the affected devices are in the U.S., according to Philips®.

In January 2022, the FDA announced that Trilogy Evo® ventilators and Trilogy Evo® repair kits not originally recalled in the July 2021 recall were added to the recalled devices list.

Recalled Philips® device brands include:

  • Aeris®
  • BiPAP A30/A40 Series Device Models®
  • BiPAP V30®
  • C-Series ASV®
  • Dorma 400 and 500®
  • DreamStation®
  • E30®
  • Garbin Plus®
  • LifeVent®
  • REMstar SE Auto®
  • SystemOne (Q-Series)®
  • Trilogy 100®
  • Trilogy 200®
  • Trilogy Evo®

Those patients who have been injured by Philips© CPAP ventilators and machines are encouraged to come forward for a free, private case evaluation that could lead the way to legal compensation.

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IS THERE A CASE?

If anyone suffers from CPAP ventilators, there may be compensation awarded.

EXPERIENCED LAWYERS

Our experts have extensive experience in CPAP machine litigation and are ready to fight in court.

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Contact us right away to set up a free and confidential case review. 

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Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Philips® or any government agency.

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