The Exactech knee recall lawsuit has generated concern and confusion among patients who have undergone knee replacement surgery. If you or a loved one has had a knee implant, it is essential to understand the reasons behind the recall, the affected products, and the potential health risks. This blog post aims to provide an overview of the Exactech knee recall lawsuit to help individuals determine if they may be impacted and what legal steps to take.

Reasons Behind the Exactech Knee Recall

The Exactech knee recall was initiated due to reports of early failure and complications associated with certain knee replacement systems manufactured by the company. These issues were primarily attributed to design and manufacturing flaws in some of their products. As a result, some patients experienced increased pain, swelling, instability, and reduced range of motion, necessitating revision surgery to correct the problems.

Affected Products

The Exactech knee recall primarily involves the Optetrak knee replacement system, specifically the tibial components used in the device. These components were reported to have a design flaw that could lead to premature wear, loosening, or failure. If you have undergone knee replacement surgery with an Exactech device, it is crucial to consult with your healthcare provider to determine if your implant is part of the recall.

Potential Health Risks for Exactech

Patients who have received an affected Exactech knee replacement device may face several health risks, including:

  1. Pain and swelling: The affected knee implant components may cause increased pain and swelling in the joint, making it difficult to perform daily activities.
  2. Instability: The loosening of the implant components may lead to instability in the knee, increasing the risk of falls and injuries.
  3. Infection: In some cases, patients may develop infections around the implant site, which can be challenging to treat and may require additional surgeries.
  4. Revision surgery: Patients experiencing significant complications may need revision surgery to remove the faulty implant and replace it with a new device. This surgery can be more complex and carries additional risks compared to the initial knee replacement.

Steps People Should Take

If you suspect that you may have been affected by the Exactech knee recall, take the following steps:

  1. Consult your healthcare provider: Speak with your surgeon or primary care doctor to determine if your knee implant is part of the recall and discuss any symptoms or concerns you may have.
  2. Monitor your symptoms: Keep track of any pain, swelling, or instability you experience, and report any changes to your healthcare provider.
  3. Obtain your medical records: Request a copy of your surgical records, including the specific implant components used during your knee replacement surgery.
  4. Seek legal counsel: If your knee implant is part of the recall and you are experiencing complications, consult with an experienced medical device attorney to discuss your legal rights and potential compensation.

Leave a Comment