Michigan Exactech Lawsuit Lawyer

Our Michigan Exactech lawsuit lawyers represent clients who have experienced problems with this knee replacement device. Patients with surgically implanted knees and ankles that have experienced serious problems after the device implant may be entitled to significant financial compensation.

Our defective medical device lawyers are available now for a free case consultation. We will determine if you qualify for a settlement from Exactech. If you have a claim, we will file it for you immediately.

• What problems are caused by the defective medical devices?
• What should patients do if they have a recalled Exactech device?
• Can I file an Exactech knee replacement lawsuit?
• Contact a Michigan Exactech Lawsuit Lawyer Today

About Exactech

Exactech is a company with its headquarters in Gainesville, Florida. Founded by orthopedic surgeons and biomedical engineers, it designs and manufacturers medical implants, instruments, and technologies. It makes joint replacement implants including for shoulder, hips, knees and ankles.

The company has over 900 employees worldwide and distributes its medical devices in more than 35 companies. It has an affiliation with the University of Florida.

About the Exactech Knee & Ankle Recall

Exactech recently issued a recall for knee and ankle replacement systems was recently announced after it was discovered that they contained a defective plastic insert component that causes them to fail prematurely. The device maker recalled total knee and ankle devices with plastic inserts packaged in non-conforming bags with a missing layer of ethylene vinyl alcohol (EVOH).

The defective medical devices have a higher and earlier than expected revision rate than expected. This can result in bone loss (osteomyelitis) and other serious issues in the knees and ankles. The company notified orthopedic surgeons and surgical centers in February 2022 so that the recall could be communicated to their patients. Exactech has set up a claims center to submit and process claims.

The company had previously recalled other products, including knee and ankle arthroplasty polyethylene inserts. These components were used in over 100,000 surgeries. The devices at issue are:

• Optetrak®
• Optetrak Logic®
• Tuliant®
• Vantage®

The device defects were caused by improper packaging of the devices in defective vacuum seal bags which resulted in oxidation of the materials. This results in significant degrading of the materials over time and affects the mechanical use of the device.

What problems are caused by the defective medical devices?

Patients with these defective knee implants and ankle implants have reported a number of medical problems. These include, but are not limited to:

• Pain and severe discomfort
• Inability to bear weight on joint
• Grinding noises and sounds in joint,
• Swelling in the knee and ankle
• Instability in the knee or ankle.

Many patients have sought additional medical treatment for these conditions, including physical therapy and pain medications. Unfortunately, many times relief can only be accomplished through revision surgery or a second joint replacement.

What should patients do if they have a recalled Exactech device?

Patients will need to verify that they do have a recalled Exactech implant device that is causing a current medical problem. It is wise to contact an experienced defective knee replacement lawyer to assist you with filing your lawsuit. To submit the claim, your lawyer will need the following information:

• Date of joint replacement surgery
• Name of the surgeon performing the joint replacement surgery
• Serial number of the implant

You likely do not have this information in your personal records. You can contact your implanting surgeon and ask what type of implant you have. The company will be providing orthopedic surgeons with the serial numbers and other patient identifiers.

In addition, our experienced defective medical device lawyers will get your medical records and surgical reports from your doctor and surgical center. We can locate all of this information and submit it along with your claim.

Can I file an Exactech knee replacement lawsuit?

Yes, if you have a recalled knee implant and have experienced pain, discomfort, swelling, and other symptoms caused by the recalled device. Because the company recalled the devices, it is unlikely that it will defend the lawsuits based on liability issues. Rather, the issue will likely be the nature and extent of your injuries and the amount of compensation to pay you for your pain and suffering.

How much are Exactech lawsuits settlements?

The amount of a settlement will depend on the severity of the harm caused by the recalled knee or ankle device. Patients who have undergone revision surgery or required a second implant will be entitled to significant compensation. Those who have experienced pain and discomfort are also entitled to a settlement and many will receive money compensation in the same range as those with replacements.

The amount of settlement compensation is determined on a case-by-case basis. Factors included in determining the amount of an Exactech settlement will include the type of harm caused by the device, the pain and suffering endured by the patient, and the medical treatment needed to reduce or eliminate the harm caused by the recalled device. Claims for medical expenses and lost income are also included in the settlement demand made to the device manufacturer.

Contact a Michigan Exactech Lawsuit Lawyer Today

If you or someone you care about has suffered harm from a recalled Exactech knee or ankle, contact our experienced Michigan defective medical device lawyers today. We will investigate your claim, get your medical records, and submit your claim for you.

We do not charge any legal fees unless you win a settlement. And, we pay all case expenses.