A knee, hip, or ankle implant promises restored mobility. But what happens when it fails prematurely? Exactech, a leading orthopedic device manufacturer, has recalled thousands of joint replacement implants due to defective packaging, leaving patients grappling with pain, revision surgeries, and uncertainty. In this blog, you will know how to determine if your implant is part of the recall and outlines clear steps to protect your health and rights. Stay informed and empowered with this guide
Understanding the Exactech Recall
Why the Recall Happened?
Exactech initiated recalls starting in August 2021, targeting knee, ankle, hip, and shoulder implants manufactured since 2004. Faulty vacuum-sealed packaging lacked a critical oxygen barrier, causing polyethylene inserts to degrade prematurely. This oxidation can lead to implant failure, pain, swelling, and the need for revision surgery. Over 147,000 knee and ankle implants and 90,000 hip implants are affected, with significant implications for patients.
Which Implants Are Involved?
The recall includes specific Exactech systems: Optetrak, Truliant, and Vantage for knee and ankle replacements, and Connexion GXL liners for hip replacements. In 2024, the Equinoxe Shoulder System was added to the recall. If you received a joint replacement after 2004, your implant might be at risk. Check the full list of affected devices on Exactech’s official recall website.
How to Check If Your Implant Is Affected?
Step 1: Gather Your Medical Records
Contact your surgeon or hospital to obtain records of your joint replacement surgery. Look for details like the implant’s brand, model, and serial number. These records are crucial for verifying if your device falls under the recall.
Step 2: Use Exactech’s Online Tool
Visit recall.exac.com and enter your implant’s serial number into Exactech’s lookup tool. This tool confirms whether your device is part of the recalled batch. If you lack the serial number, your surgeon or medical provider can assist in retrieving it.
Step 3: Monitor for Symptoms
Watch for signs of implant failure, such as persistent pain, swelling, difficulty bearing weight, or joint instability. These symptoms may indicate premature wear due to the defective packaging. Schedule a visit with your doctor for X-rays or further evaluation if you notice these issues. Exactech recall lawsuit claims often stem from these complications, highlighting the severity of the issue.
Step 4: Consult Your Surgeon
Discuss your implant status with your surgeon. They can confirm if your device is recalled and recommend diagnostic tests like X-rays to check for bone loss or implant degradation. Early detection can prevent further complications.
Next Steps If Your Implant Is Affected
Seek Medical Evaluation
Schedule an appointment with your orthopedic surgeon immediately. They may recommend monitoring with regular imaging or, in severe cases, revision surgery to replace the defective implant. Revision surgeries carry risks, so discuss all options thoroughly with your healthcare provider.
Document Everything
Keep detailed records of your symptoms, medical visits, and communications with your doctor or Exactech. This documentation strengthens your case if you pursue legal action. Note any medical expenses, lost wages, or impacts on your quality of life.
Explore Legal Options
Contact a mass tort lawyer to evaluate your eligibility for compensation. Exactech faces over 1,000 lawsuits in multidistrict litigation (MDL) in New York and state courts in Florida, with claims alleging negligence due to defective packaging. A lawyer from People For Law can guide you through filing a claim, gathering evidence, and navigating the legal process. Compensation may cover medical costs, pain, suffering, and lost income, with estimated settlements ranging from $50,000 to $300,000, depending on case specifics.
Avoid Direct Claims with Exactech
Exactech’s reimbursement program, managed by Broadspire, covers some out-of-pocket costs like copays or travel expenses. However, accepting these funds may limit your ability to file a lawsuit. Consult a mass tort lawyer before submitting a claim to ensure you don’t waive your rights to pursue broader compensation.
Stay Informed
Follow updates from the FDA and Exactech’s recall website for the latest on affected devices and litigation progress. The MDL in New York, with over 1,090 pending cases as of December 2024, continues to grow, and bellwether trials are set for 2025. Joining a lawsuit may strengthen your case as more patients come forward.
Consider Revision Surgery
If your doctor recommends revision surgery, weigh the benefits against the risks. Revision procedures are complex, often involving bone grafts due to potential bone loss from implant degradation. Ensure you understand the recovery process and long-term outcomes before deciding.
Legal and Financial Considerations
Why Legal Action Matters?
Filing an Exactech recall lawsuit holds the manufacturer accountable for negligence. Lawsuits claim Exactech knew about packaging issues as early as 2004 but failed to act until 2021. A successful lawsuit can secure compensation for medical bills, emotional distress, and reduced quality of life.
Choosing the Right Lawyer
Select a mass tort lawyer with experience in medical device litigation. Firms like People For Law specialize in Exactech cases and offer free consultations. They work on a contingency basis, meaning no fees unless you win compensation.
Act Within Time Limits
Each state has a statute of limitations, typically one to three years from the date of injury or discovery. Consult a lawyer promptly to ensure your claim is filed on time. Delays could jeopardize your ability to seek compensation.
What Will Happen In The Future?
Navigating the Exactech implant recall can feel overwhelming, but you have options. Confirm if your implant is affected, seek medical advice, and explore legal recourse to protect your health and rights. With proactive steps and expert guidance, you can address the challenges of a defective implant and move toward recovery and justice.
