If you have recently undergone a knee or ankle replacement, you may be wondering if you can file a lawsuit against the manufacturer of the device. This article will discuss how the Exactech Knee Replacement fails to function as intended, and how victims of defective implants can obtain compensation. The company has responded by saying it will issue refunds to victims. However, if you have suffered from a defective knee or ankle replacement, you should speak with a lawyer who has experience handling these cases.
Exactech knee replacement lawsuits
Thousands of consumers are suing Exactech for their defective knee Exactech Knee Recall Lawsuit replacement. This medical device is known to have an increased failure rate. These patients may experience pain and stiffness after surgery, as well as bone loss and other complications. A defect in a medical device may lead to the need for multiple revision surgeries, resulting in further financial and emotional hardship. Defective Exactech knee replacement lawsuits allege that the company should have provided warnings to consumers regarding possible problems with their product.
In addition to knee and ankle implants, patients may be entitled to compensation if their Exactech knee replacement system failed. This may result in significant pain and limited knee mobility, as well as the need for corrective revision surgery. According to the Exactech recall letter, physicians should keep a file of their patients who have had Exactech knee and ankle replacements. These doctors should closely monitor the patient’s progress to determine if a new implant is needed.
Failure of Exactech knee replacement devices
Many patients are complaining about the recalled Exactech knee replacement products, including the Optetrack and Connexion GXL acetabular liners. These knee replacement devices may be defective, causing premature failure, inflammatory response, and bone loss. Thousands of lawsuits have been filed against the manufacturer. Exactech recently expanded the recall to include polyethylene liners and components for total ankle and knee arthroplasty.
The failures are attributed to several causes, including tibial loosening, wear and tear of the devices’ components, and the cement-tibial interface. The failures force patients to undergo revision surgery to remove the defective knee implant and replace it with a new one. Revision surgeries carry a higher risk than the original implant surgery. Depending on the extent of the damage, a patient may be eligible for compensation.
Compensation offered to victims of defective implants
The recent recall of the Exactech (r) knee replacement joint involves the wear of a polyethylene insert, which can cause inflammation and even require revision surgery. Such surgeries require a much longer recovery time, more complex components, and additional surgery time. Fortunately, the manufacturer is offering compensation to victims of this faulty implant. However, the program is unlikely to cover the full cost of lost income and pain.
While Exactech has indicated that they are willing to reimburse those who have undergone the knee or ankle replacements because of their defects, these compensation offers are limited and do not adequately address the costs of future health care and medical bills. It is crucial to retain the services of a product liability attorney to ensure that you receive the maximum compensation for your injuries. It is essential that you contact an attorney as soon as you suspect a defective device has harmed you.