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Victims of severe injuries and medical conditions from recalled Phillips® brand CPAP & BIPAP devices can finally seek justice and compensation

Victims of severe injuries and medical conditions from recalled Phillips® brand CPAP & BIPAP devices can finally seek justice and compensation

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To Qualify

  • Used a Phillips CPAP or BiPAP RECALLED device for 4 Years of Longer PRIOR to 2/25/2021
  • Did not smoke while using the device
  • Diagnosed with Lung Cancer, Oral cancer, nasal cancer, larynx cancer

or

  • Diagnosed with lung injuries such as Chronic asthma, Pneumonitits, COPD & Pulmonary Fibrosis
  • Have your device number or registration details for receiving a replacement device

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.

Phillips® CPAP and ventilation machines are causing damage—including personal injuries and cancer diagnoses—that is being reported nationwide.

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

Phillips® has announced that the company is recalling between 3 and 4 million CPAP and ventilation devices due to disintegrating sound-reducing foam.

Consumers have begun to report severe side effects, including kidney/liver damage, wide-ranging chemical poisonings, and other unhealthy conditions.

Many consumers experience severe 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.

Important consumer information on recalled CPAP or BiPap Devices

Consumers had to register their recalled device to be eligible to receive a replacement device. Those who registered their recalled device received a registration number provided by Philips. Once registered Philips would have placed you on a priority list and you may now have received the replacement device.
 
If you are need to registering for a replacement deviceTo register for a replacement device, consumers have to enter their name and device Serial Number (S/N) (located on the back of the Philips recalled device), into the following Philips website:  https://www.philipssrcupdate.expertinquiry.com/?ulang=en If the Serial Number is not on the recall list, it will not allow the client to complete registration and replacement process.
 
What if I can’t find the registration number and/or serial number?
Consumers can call the Philips helpline set up for this purpose:  (877) 907-7508.
 
Clients who call the above number will be asked to verify:
  1. Last name
  2. Zip Code
  3. Last (4) digits of the phone number they used to register their device.
Alternatively, clients who lost their registration number and/or serial number and don’t want to speak to a person can log into their portal at the following website: https://www.philipspatientportal.expertinquiry.com/

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

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

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

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 identified devices list.

The USA Assistance Team believes that victims that suffered severe injuries and medical conditions due to recalled Phillips® brand CPAP & BIPAP devices should receive justice and compensation for losses.

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

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