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Millions of Americans suffer from sleep apnea, requiring sophisticated medical devices to help them sleep soundly. Philips, a major manufacturer of a wide variety of medical devices, supplies some of the most popular sleep apnea devices currently on the market. In June 2021 the FDA announced a Class I recall of certain Philips respirators, CPAP, and BiPAP machines.

A Class I recall is the most serious type of recall issued by the FDA, meaning that there is a serious probability of adverse health consequences or death connected with the use of the product. If you are one of the 3.5 million people impacted by the use of one of these devices, contact our CPAP recall lawsuit lawyers to discuss whether you may be entitled to compensation.

Why Philips CPAP Devices Have Been Recalled

The Philips devices, including the popular DreamStation CPAP and BiPAP machines, are being recalled due to problems with the polyester-based polyurethane (PE-PUR) sound abatement foam. This foam is used to reduce the noise and vibration of the device, but unfortunately, can break down over time and enter the device’s airway. When this happens, black debris may be swallowed or inhaled by the person using the device, leading to serious health issues.

You can find a list of all of the recalled devices on the FDA website, along with other information that you might find helpful. If you are currently using your device, the FDA is recommending that you contact your physician to discuss your options. While there are options available to avoid future issues, these remedies do not address the harm that may have already occurred.

Serious Health Risks Associated with the Philips BiPAP, CPAP, and Ventilator Devices

At this time, there have been more than 1,200 complaints filed regarding these devices and over 100 serious injuries reported. If you have suffered any of the following issues, we recommend that you seek immediate medical treatment and advice from your doctor regarding the continued use of your machine:

  • Skin, eye, or respiratory tract irritation
  • Headaches
  • Asthma
  • Inflammation
  • Hypersensitivity
  • Nausea or vomiting
  • Kidney or liver problems

The issues with these machines could even carry potential carcinogenic effects. Contact our Philips CPAP recall lawsuit lawyers to discuss whether your machine has been recalled and whether we can include you in the class action lawsuit we have already filed against Philips.

Philips Recall Lawsuit: Are You Entitled to Compensation?

If you have used or are currently using one of the recalled Philips BiPAP, CPAP, or ventilator devices, you may be entitled to compensation for the following:

  • Current and future medical expenses
  • Lost income
  • Your pain and suffering

Unfortunately, this is a time-sensitive matter. To discuss whether you are eligible for compensation, you should contact a CPAP recall lawyer soon as possible.

Contact Hudson Injury Firm to Learn More About Your Eligibility for Compensation Due to the Philips Recall Lawsuit

Our attorneys intend to hold Phillips accountable for the injuries and health problems caused by their devices. If you have used or are using a Philips BiPAP, CPAP, or ventilator device, you may be eligible for inclusion in our pending class action lawsuit. Call us today at 229-814-0751 or complete our online contact form to schedule a free, no-obligation consultation.