Aeris LifeVent Lawsuit | Latest Updates

Aeris LifeVent Lawsuit Overview

The Philips Aeris LifeVent lawsuit centers on serious health risks caused by degraded PE-PUR sound abatement foam in these life-sustaining ventilators. The primary allegations against Philips include manufacturing defects that allowed toxic foam particles and gases to be inhaled by patients, potentially causing cancer and severe lung injuries.

Latest Aeris LifeVent Lawsuit Updates

• July 2021 – Philips issued a voluntary recall of the Aeris LifeVent Ventilator and other ventilator models due to concerns that PE-PUR sound abatement foam could degrade, become toxic, and potentially cause cancer. The recall affects patients who depend on these devices for life-sustaining therapy, creating urgent medical and legal concerns [1].

FDA Reports and Statistics

The FDA has documented serious concerns about the recalled Philips ventilators through its adverse event reporting system. Research is actively being conducted to determine the full scope of health risks associated with inhaled or ingested foam particles from degraded PE-PUR material. The agency has confirmed that particles and gases may be released when the foam deteriorates, potentially causing both immediate respiratory issues and long-term health complications including various forms of cancer.

Aeris LifeVent Injuries & Side Effects

Patients using recalled Philips Aeris LifeVent ventilators have reported a range of serious health complications linked to the degraded foam material.

Serious side effects reported include:

• Cancer: Nasal, throat, lung, and blood cancers including multiple myeloma and leukemia
• Respiratory Complications: Lung scarring, sarcoidosis, and pulmonary fibrosis
• Immediate Symptoms: Headaches, chest pressure, irritation, and inflammation
• Toxic Effects: Various health issues from inhaling degraded foam particles and gases

Do You Qualify for an Aeris LifeVent Lawsuit?

You may qualify for an Aeris LifeVent lawsuit if:

• You used a Philips Aeris LifeVent Ventilator or other recalled Philips ventilator model
• You were diagnosed with cancer, lung scarring, sarcoidosis, pulmonary fibrosis, or other serious health complications
• Your injuries required medical treatment or hospitalization
• You can provide medical documentation linking your health problems to the use of the recalled ventilator

Evidence Required for an Aeris LifeVent Lawsuit

To pursue a successful claim, you will need:

• Medical records documenting your diagnosis and treatment
• Proof of ventilator usage including model information and treatment dates
• Documentation linking your health complications to the recalled device
• Records of medical expenses and other damages

Damages You Can Recover

Compensation in Aeris LifeVent lawsuits may include:

• Medical expenses for diagnosis, treatment, and ongoing care
• Lost wages and reduced earning capacity
• Pain and suffering from health complications
• Punitive damages for corporate negligence

Aeris LifeVent Recall Information

The July 2021 recall affects multiple Philips ventilator models including:

• Aeris LifeVent Ventilator
• A-Series BiPAP V30 Auto Ventilator, A30, A40, and Hybrid A30
• C-Series ASV and S/T AVAPS
• DreamStation models including ASV, ST AVAPS, and GO
• E30 (Emergency Use Authorization)
• Dorma 400 and 500
• Garbin Plus Ventilator
• OmniLab Advanced+
• REMStar SE Auto
• SystemOne ASV4 and Q series
• Trilogy 100 and 200 Ventilators

What Should I Do if I’m Using a Recalled Philips Ventilator?

If you or a loved one are using one of the recalled Philips ventilators, Philips says you should speak with your physician to figure out the best options for continued treatment.

Philips recognizes that alternate ventilator options for therapy may not exist or may be severely limited for patients who require a ventilator for life-sustaining therapy, or in cases where disruption is unacceptable, the recall notice states. In these situations, and at the discretion of the treating clinical team, the benefit of continued usage of these ventilator devices may outweigh the risks.

Philips has begun replacing the PE-PUR foam in the recalled machines with new material. Tell your doctor about any symptoms you have that may be related to the use of a recalled Philips ventilator.

FAQs

1. Why Were the Philips Aeris Lifevent Ventilators Recalled?

Philips Aeris LifeVent ventilators were recalled due to potential health risks from degraded PE-PUR sound abatement foam, which could release toxic particles and gases.

2. What Health Risks Are Associated With the Recalled Philips Ventilators?

Health risks associated with the recalled Philips ventilators include cancer (nasal, throat, lung, blood cancers), lung scarring, sarcoidosis, pulmonary fibrosis, headaches, irritation, and respiratory issues.

3. Which Philips Machines Are Included in the Recall?

The Philips machines included in the recall are the A-Series BiPAP, C-Series, DreamStation, Dorma, Garbin Plus, OmniLab Advanced+, REMStar SE Auto, SystemOne, Trilogy 100, and Trilogy 200 Ventilators.

4. What Should I Do if I’m Using a Recalled Philips Ventilator?

Consult your physician for continued treatment options and report any related symptoms. Philips is replacing the PE-PUR foam in affected devices.

5. Can I File a Lawsuit if I Was Harmed by a Recalled Philips Ventilator?

Yes, if you were diagnosed with cancer or suffered other injuries from a recalled ventilator, you might be entitled to compensation. Contact a specialized lawyer for a case evaluation.

Related Articles:

• Philips CPAP Machine Lawsuit
• OmniLab Advanced Plus Suit

See all related medical device lawsuits our attorneys have covered.

Get A Free Aeris LifeVent Lawsuit Evaluation With Our Lawyers

Time is limited to pursue legal action against Philips for Aeris LifeVent injuries. Each state has specific statutes of limitations that restrict how long you have to file a lawsuit after discovering your injury. Don’t wait to seek legal help, as critical evidence and your right to compensation may be at risk.

Our experienced legal team offers:

• Free, confidential consultations to evaluate your case
• No upfront costs or fees – you pay nothing unless we win
• Nationwide representation for Philips ventilator cases
• Dedicated support throughout the entire legal process

Reference:

https://www.fda.gov/medical-devices/respiratory-devices/recalled-philips-ventilators-bipap-machines-and-cpap-machines