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Alabama Zimmer Knee Replacement Lawsuit Attorney

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C.L. Mike Schmidt Published by C.L. Mike Schmidt

Zimmer Knee Replacement Lawsuit
If you or someone you know has experienced complications from Zimmer knee replacement, Schmidt & Clark, LLP, is here to help. Recognized for our expertise in plaintiff representation, our primary goal is to ensure you receive the justice and compensation you’re entitled to.

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Quick Summary

  • Understanding the Basis for Claims: Patients in Alabama have filed lawsuits due to serious complications from Zimmer knee replacements, such as device failure, infection, or the need for revision surgery. These claims often center on allegations of defective design or manufacturing, inadequate warnings, and the resulting physical and financial burdens on patients.
  • Navigating the Alabama Legal Climate: The legal landscape in Alabama for Zimmer knee replacement lawsuits is influenced by recent judgments, ongoing cases, and state-specific laws governing medical device litigation. Understanding this climate is essential for affected individuals considering legal action, as it shapes the strategies for pursuing compensation.
  • Seeking Legal Recourse: For those impacted in Alabama, seeking compensation involves documenting your medical history, understanding the statute of limitations, and consulting with a specialized attorney. A lawyer experienced in medical device litigation can offer invaluable guidance, helping to navigate the complexities of the legal process and advocating for your rights.

How S&C Can Help With Your Claim?

S&C can help with your claim by providing a robust legal strategy tailored to the specifics of your Zimmer knee replacement lawsuit. Their team of skilled attorneys is well-versed in the complexities of product liability law in Alabama. They can guide you through each step of the legal process, from initial case evaluation to potential settlement negotiations or courtroom litigation.

With S&C’s assistance, you can expect:

  • A meticulous review of your medical history and the complications you’ve encountered with your Zimmer knee implant.
  • Collaboration with medical professionals to substantiate the connection between the implant and your injuries.
  • Diligent legal action against the manufacturer to seek accountability for their defective product.

Zimmer Knee Lawsuit

Over the years, Zimmer Biomet, a key player in the orthopedic industry, has been involved in lawsuits in Alabama. The company’s knee replacement systems, including the Zimmer Persona and NexGen Knee systems, have come under scrutiny due to a myriad of complications.

From device loosening to the presence of radiolucent lines – a condition that can indicate a poorly cemented or situated knee – the lawsuits claim the issues have been significant enough to lead to a recall in 2015, just three years after the Persona Knee system got its approval.

Despite the recall, as of May 2019, the Zimmer NexGen Knee litigation still had 258 cases pending involving Nexgen flex knee and medical devices. The majority of other cases have either been dismissed, withdrawn, or resolved confidentially, with many patients having filed knee replacement lawsuits.

What Is a Zimmer Knee Implant?

According to the manufacturer, the Zimmer knee implant is an artificial knee system designed to replace a natural knee that is damaged by injury or disease [1]. However, what should have been a breakthrough in orthopedic care quickly became a source of pain for many patients.

Many of these complications, often related to attune knee replacement failure, have required complex and extensive revision surgeries, often within a relatively short period after the initial surgery. Orthopedic surgeons have identified design defects or flaws in knee replacements as the root cause of these issues.

What Constitutes a Defective Zimmer Knee Implant?

A defective knee implant that causes unreasonable danger when used constitutes a defective Zimmer knee implant in Alabama. This encompasses manufacturing defects, design defects, and a failure to warn about potential dangers adequately.

If your Zimmer knee implant has caused you harm due to some issue with its manufacturing or design, or if you were not sufficiently informed about its risks, you could be in possession of a defective product.

Component defects have raised concerns specifically for Zimmer knee and hip implants. The recall of the Persona Trabecular Metal Tibial Plate and issues with debonding related to various factors are prime examples. Remember, in Alabama, you don’t need to prove negligence to deem a product defective. All you need to demonstrate is the defective nature of the product and its unreasonable danger to users.

What Is Wrong With The Zimmer Knee Implants?

According to a 2018 research by the National Institute of Health, device loosening is what is wrong with the Zimmer knew implants. This can lead to significant discomfort and the necessity for additional knee replacement surgery [2].

This complication is particularly alarming because it undermines the stability and effectiveness of the faulty knee implant, causing patients to face unexpected pain and the prospect of undergoing another invasive procedure.

Another issue has been the development of radiolucent lines in the Zimmer Persona Knee system, which is related to the thigh bone.

These lines can indicate a poorly cemented or poorly situated knee, which can lead to pain and discomfort. In some cases, the knee pain has been so severe that it has led to legal action against Zimmer.

Reasons Behind The Recall

Various issues have triggered the recalls of Zimmer knee implant systems. One major concern has been the implant’s loosening.

According to the FDA notice, in 2015, Zimmer recalled all 11,658 of its Persona Knee tibial plate implants due to complaints of loosening. Then, in 2010, Zimmer Biomet initiated a recall of 68,000 NexGen Knee components because of premature loosening issues, leading to a flurry of lawsuits [2].

Apart from loosening, other issues, like packaging problems, have also led to recalls of failed knee replacement parts. Zimmer Biomet recalled the Gender Solutions Patello-Femoral Joint System in 2017 due to packaging issues and problems with instruments.

Between 2003 and 2013, Zimmer Biomet was one of the top knee replacement manufacturers involved in the 709 knee replacement recalls.

The Class II recall was issued after multiple complaints were filed regarding “radiolucent lines” seen on exams and the loosening of the devices. – Urs P. Wyss, Department of Mechanical Engineering at The University of Manitoba, Winnipeg

Main Side Effects Named In The Lawsuits

Now, let’s delve into the main side effects named in the Zimmer knee lawsuits. Among the top complaints are [3]:

  • Severe pain
  • Loosening of the implant
  • Decreased mobility
  • Malalignment
  • Pain with mobility
  • Poor fixation of the implant

These side effects have led to serious consequences, such as the need for revision surgery due to the device’s failure and even premature failure of the device.

In some cases, patients reported radiolucent lines seen on an X-ray of the knee, indicating poor fixation and often associated with premature failure of the device.

This has been a common complaint with the Zimmer Persona knee replacements, which have been associated with a high failure rate, leading to patient complaints and lawsuits.

How Do You Qualify for a Zimmer Knee Lawsuit?

To qualify for a Zimmer knee lawsuit, you must have received a Zimmer knee replacement component, such as those from the NexGen Complete Knee Solution or Vanguard Knee System, that was later recalled.

Eligibility for joining a lawsuit includes experiencing specific complications due to a recalled Zimmer full knee replacement system, such as joint pain, swelling, infections, nerve damage, and difficulty walking or standing.

Also, suppose you required revision surgery or another total knee replacement prematurely after the initial Zimmer knee implant. Due to the unusual need for additional surgeries, you may have grounds for a lawsuit.

The Status Of The Zimmer Knee Implant Litigation in Alabama

The current status of the Zimmer knee implant litigation in Alabama involves multidistrict litigation (MDL) and bellwether trials. MDL centralizes complex lawsuits for pretrial proceedings while keeping each lawsuit separate for trial purposes.

This approach aims to save time and money and achieve consistent outcomes across cases. MDLs are formed when the Judicial Panel on Multidistrict Litigation (JPML) assesses and approves a motion to centralize related lawsuits, deciding which federal district court will manage the proceedings.

Bellwether trials in an MDL act as test cases, giving parties an indication of the possible outcomes in subsequent trials and influencing settlement strategies and negotiations.

In Alabama, there have been several notable Zimmer knee implant cases. In 2019, Angela Owen from Hot Springs, Arkansas, filed a lawsuit in Alabama concerning the iBalance knee system. This legal action was one example of a case involving the product.

Another significant case involved Laura Woodfield, who filed a lawsuit in Alabama in 2017 involving the Persona Knee system, which had to be replaced less than five months after implantation.

These cases provide insight into the experiences of patients who have faced complications with Zimmer knee implants, including those involved in the Zimmer knee implant MDL.

Zimmer Knee Lawsuit Average Settlement Amounts in Alabama

The average settlement amounts in Alabama Zimmer knee lawsuits are complicated. Zimmer Biomet has a history of settling knee replacement lawsuits, and the terms and amounts are confidential.

This makes it difficult to estimate an average settlement value. However, it’s worth noting that settlements in other knee replacement lawsuits have reached significant figures, such as Sulzer Medica paying $1 billion to settle lawsuits over its hip and knee implants, which averaged approximately $200,000 per patient.

The value of individual settlements can differ substantially, influenced by factors such as:

  • the extent of injuries
  • the specifics of each case
  • severity of injury
  • pain and suffering
  • lost wages
  • loss of future income

Filing a Zimmer Knee Lawsuit in Alabama

If you’re considering filing a Zimmer knee lawsuit in Alabama, it’s important to consult with an experienced personal injury attorney or a law firm specializing in product liability. These professionals can guide you through the process and enhance your chances of a favorable outcome.

Alabama residents seeking legal representation for a Zimmer knee lawsuit can use attorney directories to find lawyers with significant experience in similar product liability claims.

To initiate a product liability lawsuit in Alabama, plaintiffs must sue the manufacturer based on established product liability principles to recover damages for injuries caused.

Looking at the first lawsuit filed against the DePuy Synthes’ Attune Knee System in Alabama can provide a context for Zimmer’s knee lawsuits, illustrating precedents involving artificial knee complications.

Types of Evidence To Present

Certain types of evidence must be presented when filing a Zimmer knee lawsuit. Critical evidence includes medical records documenting the need for revision surgery due to the early failure of Zimmer knee implants.

Documentation of premature loosening, such as the development of radiolucent lines in the Zimmer Persona Knee system, also serves as evidence for Zimmer knee implant failure.

Other pieces of evidence may include cases of complete debonding at the cement-implant interface that required revision knee arthroplasty.

What Is the Statute of Limitations for the Zimmer Implant Lawsuit In Alabama?

The statute of limitations for Zimmer Implant lawsuits in Alabama is typically two years from the date of injury. Understanding and adhering to this two-year legal deadline is essential, as exceeding it could forfeit your ability to file a lawsuit.

How Much Is The Zimmer Implant Lawsuit Worth in Alabama?

The worth of the Zimmer implant lawsuit in Alabama is dependent on a variety of factors. These include the severity of the injury, pain and suffering, lost wages, and loss of future income.

The severity of the injury is determined based on the medical diagnosis, medical bills, hospitalizations, and the need for medication and rehabilitation.

Other factors that may affect the value of a lawsuit include:

  • The cost associated with permanent disability care, such as nursing and home care
  • Transportation expenses
  • Rehabilitation
  • Higher medical bills and longer treatment for more extensive injuries

These factors can significantly impact the value of a lawsuit in Alabama.

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

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If you or someone you care about has suffered due to complications from a Zimmer knee implant, Schmidt & Clark, LLP is ready to lend a helping hand. Our seasoned legal team specializes in cases like yours, guiding you through the intricacies of the legal system with ease.

We’re committed to providing clear insights into your rights and evaluating your potential claim regarding Zimmer knee implant complications.

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