If you have undergone a total knee replacement surgery and have experienced pain afterward, you may want to look into filing an Exactech knee recall lawsuit. The company recently recalled more than 140,000 total knee replacement systems due to a manufacturing defect. The defect involves oxygen entering the plastic implant insert, leading to premature failure of the implanted component.
Exactech's Optetrak knee replacement implant system
If you are a victim of an Exactech knee implant system, you may want to file a lawsuit to recover damages. The company has been recalled for the Optetrak knee replacement implant system, which includes patellar and femoral caps, tibial tray, and tibial insert. This system has been known to cause problems, and there is a strong likelihood that thousands of patients have been harmed by it.
The recalled Optetrak knee replacement systems are made of polyethylene, which can oxidize if exposed to oxygen. This can lead to premature wear and damage of the plastic components. As a result, these knee replacements can cause pain, instability, and other complications.
This recall affects a class II knee replacement system. As such, it is important to speak with your doctor to ensure you received the correct implant. Failure to do so may lead to significant pain and loss of mobility. In some cases, patients may need to undergo a second surgery to replace the system. While Exactech will likely offer to cover your medical expenses, it is always wise to consult with an attorney before signing any contract. Otherwise, you could be signing away your right to a fair settlement and deserve compensation.
Manufacturing defect
A manufacturing defect in an Exactech knee replacement system can lead to significant pain, swelling, and loss of mobility of the knee. This can ultimately lead to a need for corrective revision surgery. The manufacturer is strictly liable for a design flaw that affects the safety and function of their products.
As a result of the defective design of the Exactech knee replacement system, the company has recalled the devices. Patients who have had the implants should contact the surgeon who performed the surgery. Although the surgeons were supposed to send letters to affected patients, many have moved or retired, so they may not have received the recall letters. In these cases, it is essential to consult an attorney to determine your legal rights.
The recall affects hundreds of thousands of Exactech knee and ankle replacement devices. These implants are not designed to withstand oxygen exposure and can degrade prematurely. Because these plastic products have no secondary protective layer, patients may experience serious pain and complication after the procedure.
Health consequences
Exactech has recalled hundreds of thousands of knee and ankle replacement devices, including knee replacement and ankle replacement. The reason for the recall is that some Exactech knee and ankle replacement devices failed to protect the patient's skin from oxygen exposure, which can lead to premature degeneration of the implants. This oxidation can cause pain, tissue damage, and even bone loss. As a result, patients have suffered significant health consequences and have needed revision surgeries.
Exactech has expanded its previous knee recall, and now includes polyethylene inserts packaged in non-conforming vacuum bags. These defective bags may have leaked oxygen into the devices, causing a failure to form the liners. As a result, patients who have received the recalled implants may need revision surgery. This recall has been categorized as a Class II medical device recall by the US Food and Drug Administration.
The recall relates to plastic inserts used in the Optetrak, Truliant, and Vantage knee and ankle replacement devices. Replacement inserts were shipped in vacuum-sealed plastic bags, but the oxygen caused the plastic to warp and lose its effectiveness. This resulted in worsening knee damage and significant discomfort for the patients. In addition, the recall also exposed Exactech's failure to maintain quality control over their production processes.
Class action lawsuit
Many patients have been harmed by the Exactech Knee Recall. This recall involves multiple types of recalled products that were used for knee, ankle, and hip replacements. As a result, patients have taken legal action in order to protect their health and rights.
Patients who have received an Exactech knee replacement may be able to file a product liability lawsuit against the company. If their implant failed, they could be awarded damages for pain and suffering, medical expenses, and lost wages. In addition to compensation for medical costs, these lawsuits hold the Exactech company responsible for the harm their products have caused.
Exactech has stated that it will reimburse affected patients. However, if you have suffered serious pain due to your defective device, you may have to undergo revision surgery or even get a new implant. Regardless of the type of Exactech knee replacement device you received, it is important to retain a qualified, experienced attorney to represent your case.