The Schmidt National Law Group is no longer accepting these cases.
In August 2020, Exactech Inc., a Florida-based medical device manufacturer, issued a voluntary recall of the OPTETRAK knee / ankle implant system. The recall was issued due to a defect in the device’s tibial component, which can cause several serious side effects, including pain, swelling, and difficulty walking.
Patients who have received a hip, knee, or ankle implant since 2004 that was manufactured by medical device company Exactech, please contact us and your physician for guidance on what you need to know and do to prevent further injury and to make an Exactech implant recall claim.
This recall may affect hundreds of thousands of people across the U.S. who may have experienced premature wear of the plastic insert of the hip, knee, or ankle replacement that can lead to the need for additional surgery (also known as revision surgery).
In the wake of the recall, many former recipients of the OPTETRAK knee implants have filed lawsuits against Exactech, seeking financial compensation for the medical expenses and emotional suffering caused by the defective device. On this page, we will explore the legal implications of the Exactech knee recall lawsuit and discuss what consumers need to know about their rights in the Exactech recall.
Overview of the Exactech Recall Lawsuit
The Exactech knee recall lawsuit is a multi-district litigation (MDL) that has been filed against Exactech Inc. by former recipients of the Connexion GXL implant system. The lawsuit alleges that Exactech failed to adequately warn consumers of the risks associated with the defective device, and seeks financial compensation for the medical expenses and emotional suffering caused by the defect. The Exactech recall lawsuit includes both individual and class action claims, with a wide range of plaintiffs from all over the country.
What is a Multi-District Litigation (MDL)?
An MDL is a type of legal proceeding in which separate lawsuits with similar claims are consolidated into a single action. An MDL is typically used in cases involving defective products, medical malpractice, or other mass torts. In the Exactech recall lawsuit, the MDL allows the plaintiffs to pool their resources to build a stronger case against Exactech. It also streamlines the legal process, as all of the plaintiffs’ claims will be handled in a single court.
Legal Implications of the Exactech Recall
The legal implications of the Exactech recall are significant. The lawsuit seeks financial compensation for the medical expenses and emotional suffering caused by the defective device, as well as punitive damages for Exactech’s negligence.
The Exactech recall lawsuit also seeks to hold Exactech liable for the costs associated with having to replace the defective device. If the plaintiffs succeed in their lawsuit, Exactech could be forced to pay out millions of dollars in damages via cash settlements.
The Exactech knee recall lawsuit also has implications for other medical device manufacturers. The success of the Exactech recall lawsuit could set a precedent for other manufacturers of defective medical devices, which could lead to more stringent regulations for the medical device industry.
Consumer Rights in the Exactech Recall Lawsuit
As a former recipient of the OPTETRAK knee implant system, you are entitled to certain rights in the Exactech knee recall lawsuit. The first right is the right to seek financial compensation for the medical expenses and emotional suffering caused by the defective device. You also have the right to join the class action lawsuit against Exactech, which could provide you with additional financial compensation. Finally, you have the right to seek punitive damages against Exactech for its negligence in failing to warn consumers of the risks associated with the defective device.
The OPTETRAK Knee and its Role in the Exactech Recall
The OPTETRAK, OPTETRAK Logic, and TRULIANT knee implant systems are types of knee replacement devices manufactured by Exactech Inc. The device is designed to replace a damaged knee joint, allowing the user to regain mobility and reduce pain. Unfortunately, the device is defectively designed, leading to a number of serious side effects, including pain, swelling, and difficulty walking.
If you are experiencing any of the following symptoms, your Exactech implant may be one of the recalled devices and could have failed due to degradation or deterioration:
- Chronic or worsening pain in hip, knee or ankle
- Feeling of loosing or grinding
- Instability or limited mobility
- Osteolysis, or degeneration of bone tissue
- Device failure or malfunction
- Revision surgery due to any of the above
The defective device is the primary cause of the Exactech knee recall lawsuit. Exactech failed to warn consumers of the risks associated with the device, leading to several lawsuits against the company.
Legal Representation for Exactech Knee Recall Victims
If you are a former recipient of the Exactech knee or ankle implant system, you may be eligible to join the Exactech recall lawsuit. To do this, you will need to speak with our experienced attorneys who specializes in product liability law. The Schmidt National Law Group can help you understand your rights in the lawsuit, and assist you in filing a claim against Exactech. It is important to note that the Exactech knee lawsuit is a complex legal matter, and it is in your best interest to seek the advice of an experienced lawyer.
Financial Compensation for Exactech Recall Victims
If you are a former recipient of the OPTETRAK knee implant system and have been affected by the Exactech recall, you may be eligible to receive financial compensation. This recall lawsuit seeks to hold Exactech accountable for the medical expenses, emotional suffering, and other costs associated with the defective device. If the plaintiffs are successful in their lawsuit, Exactech could be forced to pay out millions of dollars in damages.
In addition to the financial compensation sought in the Exactech recall lawsuit, former recipients of the Connexion GXL knee or ankle implant system may also be eligible for compensation from Exactech’s recall program. This program provides reimbursement for the cost of surgery, medical supplies, and other expenses associated with the recall.
Solutions for Exactech Recall Victims
If you are a former recipient of a Exactech knee or ankle implant system, the first step you should take is to speak with an experienced attorney who specializes in product liability law. An experienced attorney can help you understand your rights in the Exactech knee recall lawsuit, and assist you in filing a claim against Exactech.
In addition to legal representation, you should also consider joining the Exactech recall program. This program provides reimbursement for the cost of surgery, medical supplies, and other expenses associated with the recall. You should also contact your doctor to discuss the risks associated with the defective device and any possible treatments or remedies.
Finally, if you have suffered any medical complications as a result of the defective device, you should speak with a medical malpractice attorney. A medical malpractice attorney can help you determine if you are eligible for compensation from Exactech or from any other third parties who may be liable for the defect.
Conclusion
The Exactech knee recall lawsuit has significant legal implications for both Exactech and the medical device industry as a whole.
If you have experienced premature wear of any of these Exactech Hip, Knee or Ankle products contact us today for a free injury case review at 1-800-631-5656 or use the claim form on the right side of this page, we intend to hold the manufacturer responsible for the failure of its medical devices.
Exactech Recall Lawsuit for knee or ankle implants page updated on February 23, 2023.