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Health Dangers From Using A Recalled Phillips® Brand CPAP & BiPAP Devices

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

Severe Injuries And Medical Conditions From Recalled Phillips® Brand CPAP & BiPAP Devices

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

Those eligible:

  • Must have used a RECALLED Phillips® brand CPAP and BiPAP devices for four (4) years or longer before Thursday, February 25, 2021 (09-25-2021);
  • Must not have smoked while using the device; and,
  • Must have been diagnosed with cancer of the:
    • Lungs;
    • Mouth;
    • Nose; or,
    • Larynx;
  • Or, must have been diagnosed with lung injuries such as;
    • Chronic asthma;
    • Pneumonitis;
    • COPD; or,
    • Pulmonary fibrosis.

Those eligible must have the device number or registration details to receive 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.

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Important Consumer Information On Recalled Phillips® Brand CPAP and BiPAP Devices

Consumers should have registered their recalled devices to receive a replacement.

Those who registered their recalled device should have received a registration number provided by Phillips®.

Once registered, Phillips® should have placed you on a priority list, and you may have already received the replacement device.

“What if I need to register for a replacement device?”

To register for a replacement device, consumers should enter their name and device serial number (S/N) located on the back of the Philips recalled device into the following Phillips® website:  https://www.philipssrcupdate.expertinquiry.com/?ulang=en

The client cannot complete the registration and replacement process if the serial number is not on the recall list.

“What if I can’t find the registration or serial numbers?”

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:

  • Last name
  • Zip Code
  • The last four (4) digits of the phone number used to register the device.

Alternatively, clients who have lost their registration or serial numbers and don’t wish to speak to a live agent can log into their portal at the following website: https://www.philipspatientportal.expertinquiry.com/.

Eligible victims are encouraged to request a free, private case evaluation by our experienced legal staff with the potential for compensation and justice.

Find Out if You Qualify

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Severe Injuries And Medical Conditions From Recalled Phillips® Brand CPAP & BiPAP Devices

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

Those eligible:

  • Must have used a RECALLED Phillips® brand CPAP and BiPAP devices for four (4) years or longer before Thursday, February 25, 2021 (09-25-2021);
  • Must not have smoked while using the device; and,
  • Must have been diagnosed with cancer of the:
    • Lungs;
    • Mouth;
    • Nose; or,
    • Larynx;
  • Or, must have been diagnosed with lung injuries such as;
    • Chronic asthma;
    • Pneumonitis;
    • COPD; or,
    • Pulmonary fibrosis.

Those eligible must have the device number or registration details to receive a replacement device.

shutterstock_791903353-min

Important Consumer Information On Recalled Phillips® Brand CPAP and BiPAP Devices

Consumers should have registered their recalled devices to receive a replacement.

Those who registered their recalled device should have received a registration number provided by Phillips®.

Once registered, Phillips® should have placed you on a priority list, and you may have already received the replacement device.

“What if I need to register for a replacement device?”

To register for a replacement device, consumers should enter their name and device serial number (S/N) located on the back of the Philips recalled device into the following Phillips® website:  https://www.philipssrcupdate.expertinquiry.com/?ulang=en

The client cannot complete the registration and replacement process if the serial number is not on the recall list.

“What if I can’t find the registration or serial numbers?”

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:

  • Last name
  • Zip Code
  • The last four (4) digits of the phone number used to register the device.

Alternatively, clients who have lost their registration or serial numbers and don’t wish to speak to a live agent can log into their portal at the following website: https://www.philipspatientportal.expertinquiry.com/.

Eligible victims are encouraged to request a free, private case evaluation by our experienced legal staff with the potential for compensation and justice.

100% Free & Secure Case Evaluations

Answer a few basic questions to get started

We’ll ask specific questions to understand the situation, the injuries, and other vital info to help determine the next steps.

Receive a confidential case evaluation

A qualified legal team led by a personal injury attorney will consider the facts of the case and the potential for compensation.

Have an individual claim filed for compensation

Those that qualify will have an individual claim filed in a court of law for the justice and compensation they deserve.

Don’t suffer personal injury from recalled Phillips® brand CPAP and BiPAP devices in silence any longer—we fight for justice!

Victims of severe injuries and medical conditions from recalled Phillips® brand CPAP & BiPAP devices should have every opportunity to address the company in court for the compensation and justice they deserve.

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

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