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Lawsuits Filed After Heart Valves Failed

The Abbott Trifecta aortic heart valve is a medical device used in heart surgeries to replace damaged or diseased aortic valves. Designed to restore normal blood flow, the valve was intended to improve the quality of life for patients suffering from conditions like aortic stenosis. However, many individuals have experienced severe complications due to premature valve failure, including valve leakage and the need for additional surgeries. These complications have led to lawsuits against Abbott Laboratories, alleging that the company marketed a defective product and failed to warn patients about the associated risks.

If you or a loved one has experienced complications after receiving the Abbott Trifecta valve, you may be entitled to compensation. At Law Experts LLP, our Abbott Trifecta Valve defect attorneys are committed to helping individuals affected by defective medical devices seek justice and hold manufacturers accountable.

What is the AbbottTrifectaValve?

The Abbott Trifecta valve is a biological aortic valve replacement made from porcine (pig) tissue and mounted on a metal frame. It is designed to replace the aortic valve, allowing for improved blood flow and heart function. However, many patients have reported premature structural deterioration of the valve, leading to serious complications that require additional surgery.

These complications have raised concerns about the safety and durability of the Abbott Trifecta valve, prompting legal action from patients who have suffered significant harm due to the device’s failure.

Abbott Trifecta Valve Complications and HealthRisks

The primary issue with the Abbott Trifecta valve is its tendency to fail prematurely, leading to serious health risks. Some of the most common complications associated with the device include:
  • Valve Leakage (Regurgitation): Many patients have experienced valve leakage, where blood flows back into the heart because the valve does not close properly. This condition can lead to heart failure and require urgent medical attention.
  • Structural Deterioration: The biological tissue in the Trifecta valve can deteriorate prematurely, causing the valve to fail earlier than expected. This may lead to the need for repeat surgeries to replace the defective valve.
  • Repeat Surgeries: When the Trifecta valve fails, patients often require additional surgeries to replace or repair the valve. These surgeries carry risks such as infection, blood clots, and other complications.
  • Heart Failure: Valve failure can place significant strain on the heart, potentially leading to heart failure—a life-threatening condition that requires immediate medical intervention.
  • Stroke and Blood Clots: Patients with valve malfunction are at an increased risk of developing blood clots, which can travel to the brain and cause a stroke, resulting in long-term disability or death.

These complications can have devastating effects on patients’ health and quality of life, requiring ongoing medical treatment and repeated hospitalizations.

Allegations in the AbbottTrifectaValveLawsuits

The lawsuits filed against Abbott Laboratories are based on several key allegations, including:

  • Defective Design: Plaintiffs argue that the Trifecta valve is defectively designed, making it prone to early failure and valve leakage. The lawsuits allege that the design flaws have led to severe health complications for many patients.
  • Failure to Warn: The lawsuits claim that Abbott Laboratories failed to provide adequate warnings to patients and healthcare providers about the risks of premature valve failure, including the likelihood of needing additional surgeries.
  • Negligence: The lawsuits accuse Abbott of negligence in the design, testing, and marketing of the Trifecta valve. Plaintiffs argue that the company did not do enough to ensure the safety and reliability of the valve before making it available to patients.
  • Breach of Warranty: Many lawsuits include claims of breach of warranty, alleging that Abbott failed to deliver on its promises regarding the durability and safety of the Trifecta valve.

Who Can File an AbbottTrifectaValveLawsuit?

Unfortunately, numerous people have been negatively affected when their hernia mesh implant failed, leading to significant injuries and additional surgical procedures. Counterfeit surgical hernia mesh products, defective product designs, defective product manufacturing, and improper or incorrect product labeling are a few of the problems that have led to individuals filing lawsuits against the makers and manufacturers of specific hernia mesh brands. Some of the brands at the heart of hernia mesh lawsuits include:

  • Atrium
  • Bard Davol
  • Ethicon
  • Covidien

Additionally, many hernia mesh products have been the subject of U.S. Food and Drug Administration recalls, including:

Defective and improperly labeled hernia mesh implants can cause ongoing medical problems and complications. Those impacted by defective products may be able to seek compensation from the manufacturer for their injuries.

Compensation Available in AbbottTrifectaValveLawsuits

Patients who file lawsuits against Abbott Laboratories for complications related to the Trifecta valve may be entitled to various forms of compensation, including:

How Law Experts LLP Can Help

At Law Experts LLP, we understand the life-altering impact that defective medical devices can have on patients and their families. Our experienced legal team is dedicated to helping individuals who have been harmed by the Abbott Trifecta valve seek justice and hold the manufacturer accountable for their defective product. We will work with you to investigate your case, gather the necessary evidence, and build a strong legal claim on your behalf.

Get Your Free AbbottTrifectaValveLawsuit Evaluation

If you or a loved one has experienced complications related to the Abbott Trifecta valve, the mass tort attorneys at Law Experts LLP are prepared to help you get the justice you deserve. Take the questionnaire on this page to find out if you qualify for a lawsuit.

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