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Arkansas Impella Heart Pump Lawsuit in 2024 (Latest Updates)

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Quick Summary

  • If you’ve experienced complications from the Impella heart pump in Arkansas, you should be aware of the serious health repercussions that have led to ongoing lawsuits. The Arkansas Impella heart pump lawsuit is unraveling the serious health repercussions faced by patients.
  • This article breaks down key lawsuit details, expected outcomes, and critical steps for affected individuals seeking justice without complicating your understanding with dense legal wording.
  • If you or a loved one has suffered due to complications with the Impella heart pump, Schmidt & Clark, LLP, stands ready to assist. Our firm is renowned for its proficiency in plaintiff representation, and we are dedicated to ensuring you receive the justice and compensation you rightfully deserve.

How S&C Can Help With Your Claim?

S&C can help with your claim by guiding you through the complexities of product liability claims, providing support with mounting medical expenses, and representing your interests in class action lawsuit cases after a medical device failure.

Our law firm, S&C, is committed to amplifying your concerns and advocating for your right to compensation through:

  • Expert legal guidance on product liability claims
  • Assistance with medical expenses
  • Representation in class action lawsuits

Impella Heart Pump Lawsuit

The Impella heart pump, an advanced medical device approved by the FDA, is now the subject of intense scrutiny and legal action. Designed to be a lifeline for patients with acute heart failure, these devices have, in some cases, led to heart wall tears and pump catheter-related complications.

FDA recalls, and subsequent reports of serious injuries and deaths have led to a slew of product liability lawsuits against Abiomed, the manufacturer of these defective medical devices.

The ensuing legal battles are not just about compensation – they’re a fight for accountability, patient safety, and disease control.

What Is an Impella Heart Pump?

An Impella heart pump is an innovative medical device designed to be inserted into the heart’s left ventricle through the blood vessels. Its critical function is to aid blood flow during percutaneous coronary interventions or open heart surgery.

However, the flip side of this innovation is a dark tale of design flaws and inadequate warnings that have led to devastating outcomes. It’s a stark reminder that medical advancements come with the heavy responsibility of ensuring patient safety above all else.

Reasons Behind The Recall

According to the FDA, when the agency raises the highest level alert—the Class I recall—it signals a clear and present danger. For the Impella heart pumps, it was the unreported risks of heart wall perforation that rang alarm bells [1].

Abiomed’s delayed reporting of these life-threatening conditions to the FDA resulted in urgent medical device corrections, but for some, the warnings came too late, even for FDA-approved devices.

Failure to warn of defects has become a central issue in ongoing product liability litigation. This spotlights the dire consequences of a medical device company not fully disclosing potential risks associated with faulty medical devices, as required by product liability laws. This has led to an increasing number of product liability lawsuit cases.

Side Effects of Impella Heart Pump

The side effects of the Impella heart pump include serious medical conditions such as heart wall perforations and severe hypertension. These complications have had significant impacts on patients’ health and have been the subject of considerable concern.

According to Abiomed, these side effects may include [2]:

  1. Bleeding at the insertion site
  2. Infection
  3. Blood vessel damage
  4. Heart rhythm disturbances
  5. Damage to the heart valves
  6. Stroke
  7. Blood clots
  8. Kidney damage
  9. Complications related to anesthesia or sedation

The device, intended to prevent heart attacks and assist in recovery from cardiogenic shock, has instead been linked to a number of experienced complications and fatalities, leaving a trail of questions and a demand for answers.

Ventricular perforation is a rare complication during a high-risk percutaneous coronary intervention (PCI) when supported by Impella® (Abiomed). However, instrumentation of the left ventricle several days after transmural infarct potentially increases susceptibility for perforation – Ismael A Salas de Armas (MD), Assistant professor at McGovern Medical School at The University of Texas Health Science Center at Houston (UTHealth)

How Do You Qualify for an Impella Heart Pump Lawsuit?

To qualify for an Impella heart pump lawsuit, you must demonstrate a causal link between the defective medical device and your injury, construct a narrative that highlights negligence and the resulting harm, and prove that product defects were directly responsible for your suffering.

Additionally, it is crucial to meticulously document every aspect of your medical journey, as this will be pivotal in building your case.

The Status Of The Impella Heart Pump Lawsuit Litigation in Arkansas

In Arkansas, the legal proceedings for Impella heart pump cases are part of a larger body of mass tort litigation. These cases focus on individual claims for compensation and the specific circumstances of each plaintiff’s experience.

The status of Impella heart pump lawsuit litigation in Arkansas is continually evolving. Individuals who have experienced complications or adverse effects from the Impella heart pump may be pursuing legal action to seek compensation for their damages.

This litigation may involve claims related to the device’s alleged defects, inadequate warnings, or failure to perform as intended, leading to harm or injury.

As experienced attorneys, we closely monitor the progress of such products liability litigation to provide informed guidance and representation to affected individuals in Arkansas and beyond

Impella Heart Pump Lawsuit Settlement Amounts in Arkansas

The Impella heart pump lawsuit settlement amounts in Arkansas vary and depend on various factors, including the extent of harm caused by the device, individual medical expenses, lost wages, pain and suffering, and other relevant considerations.

Settlement amounts are typically negotiated between plaintiffs and defendants or determined through legal proceedings, such as trials or mediation. As legal proceedings unfold, settlement amounts may be disclosed as part of the resolution process.

Our legal team in Arkansas is dedicated to advocating for fair compensation for individuals affected by Impella heart pump complications and ensuring their rights are protected throughout the litigation process.

Filing an Impella Heart Pump Lawsuit in Arkansas

Taking the first step to file an Impella heart pump lawsuit in Arkansas is a move towards reclamation – a chance to hold accountable those responsible for the harm caused. It begins with the drafting of a complaint, a narrative that weaves together the facts, the law, and the pain of the experience.

It’s a journey through the legal system that requires precision, evidence, and a clear understanding of where and how to navigate the courts.

Types of Evidence To Present

Building a solid case in an Impella heart pump lawsuit hinges on presenting clear and convincing evidence.

This includes:

  • Documenting medical complications through comprehensive medical records
  • Securing expert testimonies to elucidate the device’s malfunction
  • Gathering photographic evidence of physical injuries
  • Maintaining detailed records of all healthcare provider interactions
  • Accounting for all financial losses as a result of the heart pump’s issues

Each type of evidence contributes to a comprehensive view of the events and supports the claim of harm caused by the device. Together, these elements form the foundation of a legal argument aimed at achieving a just outcome.

What is the Statute of Limitations for the Impella Heart Pump Lawsuit in Arkansas?

The statute of limitations for the Impella heart pump lawsuit in Arkansas is set at two years, a critical period within which affected individuals must file their claims.

This legal deadline underscores the importance of taking prompt action to address the harm caused by medical malpractice, including injuries from defective medical devices like the Impella heart pump.

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See all related medical device lawsuits our attorneys covered so far.

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Have you or a loved one suffered severe pain or injury from a defective medical device?

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At Schmidt & Clark, LLP we stand with you in these trying times. Should you or someone close to you have endured complications from the Impella heart pump, we urge you to get in touch.

Our skilled team is well-versed in such matters and will navigate you through each step of the legal process. We are committed to demystifying your legal rights and determining your potential for filing a lawsuit related to applesauce lead contamination.

We offer free consultations and operate on a contingency fee basis, meaning we only receive payment if we win your case.

Reference:

  1. https://www.fda.gov/medical-devices/medical-device-recalls/abiomed-recalls-instructions-use-impella-left-sided-blood-pumps-due-perforation-risks
  2. https://www.abiomed.com/important-safety-information

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