Once you have hip problems, you start to realize how important they are to the quality of your life. If you have suffered a hip injury in a slip and fall, a car accident, or some other traumatic event hip replacement surgery might end up being a necessity. Often, there’s a good chance your doctor would recommend you to have a hip replacement once the problems start impacting your day-to-day tasks. It can be a relief to get back to life without hip problems, but now, an Exactech hip recall has been reported. It’s perfectly understandable to learn about this Exactech hip replacement recall and have questions to protect yourself if your doctor used the Exactech Connexion GXL liner during your hip replacement surgery. An experienced hip replacement recall lawyer near you can help answer those questions and see if you are eligible for an Exactech hip replacment lawsuit.
The recall was initiated when it became apparent that the Exactech Connexion GXL liner sold under the names Novation, Acumatch, and MCS was breaking down quicker than similar medical devices. Due to the deterioration occurring at a faster pace, individuals with these particular hip replacement devices used during their hip replacement surgery would have to have a second surgery to correct the problem that wouldn’t have been necessary if the device wasn’t defective. Researchers studying these devices believe that this was caused by the design of the hip replacement device, the manufacturing process itself, or some problem in how the device was packaged. After discovery, all of the Exactech Connexion GXL liners have been recalled. Patients who had this device implanted during their hip replacement surgery are being contacted by their surgeons for follow-up. During these follow-ups, the surgeons are looking to determine whether or not the liner in the implanted device is beginning to degrade. In addition, they are looking to decide on the proper next steps for medical treatment based on the device’s condition. Often, all that is required is an X-ray to determine the current state of the device used in your hip replacement.
Due to the material of the liner breaking down, debris from it is left in the space surrounding the prosthetic. This space also has contact with bone, soft tissue, and muscles, where they all come together for the hip to work correctly. This debris can be dangerous as they are toxic and can cause the muscles, bone, and soft tissue to become necrotic and die off, leading to severe health complications.
There are several symptoms you may be experiencing that could be due to your hip replacement beginning to deteriorate or already being degraded. These include:
In addition, if you have been told that you need revision surgery or already received revision surgery, it may have been due to a defect in the medical device. Also, if you’ve been diagnosed with Osteolysis, which is when the periprosthetic bone tissue has been damaged or destroyed, it could have been caused by a defective hip replacement device.
If you believe that you may have had an Exactech Connexion GXL liner implanted during your hip replacement surgery, you should contact your doctor right away to schedule an appointment to be seen whether you are experiencing problems or not.
You may be eligible for compensation due to the Exactech hip replacement lawsuit. Your best course of action is to speak with an experienced attorney near you that is familiar with the process of medical device recall lawsuits and has gotten results. When a medical device fails to live up to expectations, it can have devastating impacts on your health and quality of life.
Here at Glover Law Firm Accident & Injury Lawyers, we have the experience necessary to help you with your Exactech lawsuit. Don’t wait to learn more about the Exactech hip lawsuit and how you can move forward. Set up a free case consultation today.