Exactech lawsuits relating to knee, hip and ankle devices have been filed in recent years, causing some to question the safety of these products.
Surgery is extremely important and very invasive, so when something goes wrong, it can have devastating consequences.
Faulty Exactech implants and devices are the subjects of a number of these lawsuits, with patients claiming that they have suffered serious complications as a result.
If you or someone you love has been affected by an Exactech device, it is important to understand your legal rights.
You may be able to file a lawsuit against the company to recover compensation for your injuries.
Thousands of people who had Exactech knee and ankle replacements may have been injured by defective inserts and liners or needed further surgery to remove them.
To date, there have been Exactech recalls for several thousand knees and ankle inserts that could be defective, as well as the discontinuation of a type of hip liner due to its potential early wear-out.
A defective Exactech implant can cause serious injuries, requiring painful and expensive revision surgery to fix, hence the increase in lawsuits.
No, there isn’t a specific Exactech knee replacement lawsuit.
Rather, there is a lawsuit about general joint replacement surgery, including various cases about Exactech knee implant defects.
In this lawsuit, some patients have alleged that they experienced complications and problems due to their Exactech knee replacement surgery, while others have made claims about their hip or ankle implants.
This lawsuit is currently ongoing, so to learn more about your eligibility, you can use our chatbot below.
Yes, there is a class action Exactech lawsuit in New York.
Out of the 75 Exactech lawsuits filed in federal court, more than one-third take place in the Eastern District of New York, where these lawsuits are being transferred to as of October 2022.
Combining these cases into a class action lawsuit will make it easier for the court to hear and manage them and will likely lead to a more efficient process overall.
Exactech has recalled potentially defective models of their joint inserts and replacements, leading to lawsuits with patients who had already been operated on with these devices.
Patients being impacted by the issue stated that they needed revision surgery either because their devices failed too early or had been recalled post-surgery when it was too late.
In some cases, they allege that poor manufacturing of their Exactech knee, hip and ankle replacements allowed the liners to be exposed to oxygen, which led to them wearing out much faster than anticipated and causing injuries in the process.
The Exactech CEO is currently Jeffrey R Binder, although the company was founded by Gary Miller, Bill and Betty Petty in 1985.
Their goal was to administer better care to patients with injuries or chronic conditions such as arthritis.
In the present day, Exactech, Inc. is a medical device company that designs, develops, and markets orthopedic implant devices, related surgical instruments, biological materials and services to hospitals and physicians.
Headquartered in Gainesville, Florida, the company has over 1000 employees.
No, Exactech has been a privately held company since its merger with TPG Capital.
This means that the company is not publicly traded and does not have to disclose certain information to the public, as a publicly traded company would.
Before the lawsuits, Exactech had an excellent reputation.
They were known as a company that cared about its patients and provided high-quality products.
However, in recent years, the company has been involved in lawsuits and recalls of its products, invariably resulting in damage to its reputation.
You can do two things to find out if your knee replacement has been recalled.
Firstly, you can check the FDA website, which has a list of all medical devices that have been recalled in a database.
Secondly, you can call your surgeon’s office and ask if they have any information on the device.
However, if the knee replacement recall is urgent, then your surgeon will likely call you.
If your knee replacement has been recalled, it is crucial to seek medical attention as quickly possible, as there may be health risks associated with the device.
In the case of the Exactech implant recall lawsuits, the manufacturers themselves have warned surgeons of the potential problems associated with some of their devices.
Exactech recalled all units of its OPTETRAK Comprehensive Knee System due to safety concerns.
The recall includes any knee or ankle polyethene inserts that were packaged in certain vacuum bags.
On August 11, 2022, Exactech warned surgeons that these bags—which did not meet the necessary specifications and could let oxygen damage device liners—might impact even more devices than what was originally thought.
They also advised that patients with the recalled devices would likely need revision surgery as a result.
Exactech issued a warning in August of 2022, which stated that any surgeons who had implanted Connexion GXL liners at any point since 2004 may have patients who were harmed as a result.
The previous warning only applied to those surgeons that had implanted the said liners between 2015 and 2021.
The FDA classified this action as a class II recall, which means that there is a potential for temporary or reversible health effects from exposure to the product.
However, the probability of serious health consequences is low.
If you have had an Exactech knee replacement system since 2010, it is important to check if your device is impacted by the recall.
If it is, you should seek medical attention as soon as possible.
Find out how you can join the Exactech recall lawsuit by using our chatbot service below.
Patients with Exactech knee and ankle implants who have been injured by the recalled devices may be wondering how much their case is worth.
And while there is no easy answer when it comes to calculating a settlement, victims of Exactech implant defects can certainly expect to receive compensation thanks to the Exactech lawsuit.
Settlement amounts for the Exactech lawsuit are still in speculation, but lawyers expect the compensation to correlate to the type of Exactech implant the patient received.
That means Exactech knee and ankle implants will have different average settlements.
It’s estimated that lawsuit settlements for defective Exactech knee replacement systems will be between $70,000 and $150,000.
Ankle replacement lawsuit settlement may be slightly higher, from $90,000 to $175,000.
All this is based on previous payouts in other cases involving these kinds of injuries.
Knee and hip replacements are currently the most common joint replacements, as nearly a million Americans have a knee or hip replacement each year.
Although knee replacement surgery and hip replacement surgery are most prevalent, procedures such as shoulder and ankle surgery are also on the rise.
The number of procedures and materials used to make artificial joints varies, depending on the joint being replaced.
For example, knee and ankle replacements typically use a metal alloy for the artificial joint, while hip replacements may use either a metal or ceramic ball.
In the best cases, patients who undergo joint replacement surgery typically experience pain relief and increased mobility afterwards, helping them to return to their daily activities.
This type of surgery is performed when a previous surgery did not achieve the desired results or when complications from the original surgery arise.
It can involve correcting bone alignment, implant placement, and soft tissue issues.
Patients who undergo corrective revision surgery often have significant pain and disability prior to the procedure, and the goal of surgery is to relieve these symptoms and improve function.
However, corrective revision surgery is often more complex than the original surgery, and patients may require a longer hospital stay and recovery period.
There is also a higher risk of complications, such as infection.
For these reasons, it is important to consult with an experienced orthopedic surgeon before undergoing any type of revision surgery.
Knee replacement surgery is a procedure that involves replacing the damaged or diseased joint surfaces of the knee with new artificial joint surfaces.
In some instances, medical devices called implants are used to replace damaged joint surfaces.
The most common type of knee replacement surgery is total knee replacement.
In this procedure, both the femoral (thigh bone) and tibial (shinbone) surfaces of the knee are replaced with artificial joints.
Partial knee replacement is another type of replacement surgery, but in this procedure, only one of the joint surfaces is replaced rather than both.
Although this surgery can be performed on patients of any age, it is most commonly performed on patients who are 60 years of age or older.
This type of surgery, also called ankle arthroplasty, is a procedure to remove damaged bone and cartilage from the ankle joint and replace it with an artificial joint.
An ankle implant is made of metal and plastic and is intended to restore the function of the ankle joint.
There are two (2) main types of ankle replacement surgery:
A mobile-bearing ankle replacement implant system has a plastic or metal tray that is inserted into the ankle bones.
This type of implant allows the ankle to move more freely.
A fixed-bearing ankle replacement has a metal plate that is screwed into the ankle bones.
Ankle arthritis is far less common than knee or hip arthritis, so there are generally fewer ankle surgeries.
Still, the most common type of ankle arthritis is osteoarthritis, which is caused by the wear and tear of the cartilage that cushions the joints.
In many cases, the decision to have this surgery is usually made after other treatments, such as physical therapy, have failed to relieve pain.
Problems can arise with any type of surgery, and ankle replacement surgery is no different.
Generally, the most common issue after ankle replacement surgery is the instability of the ankle joint.
This can occur if the ligaments that support the ankle are damaged or if the artificial joint becomes loose.
Patients who have this problem may need to undergo revision surgery to correct it.
Other common problems after surgery include pain, infection, and blood clots.
However, problems resulting from premature wear are usually a result of manufacturing defects and not due to patient error.
This is why many with these types of issues often seek the help of an experienced attorney who can help them recover damages from manufacturers such as Exactech.
Hip replacement surgery is a procedure in which the hip joint is removed and replaced with an artificial implant.
Hip replacements are usually performed to alleviate pain and lessen the disability caused by arthritis or other conditions that affect the hip joint.
A hip implant consists of a metal ball that replaces the upper end of the thigh bone (femur) and a socket that replaces the cup-shaped hip bone (acetabulum).
The new joint can be made from metal, plastic or ceramic materials.
In most cases, post-hip-surgery patients are able to return to their previous level of activity and pain relief is significant.
However, complications can occur with any surgery, and hip replacement surgery is no exception.
In some cases, the new hip joint may dislocate, break or wear down over time.
Infection and nerve damage are other potential complications.
Because of these risks, patients should consult with their doctor to see if hip replacement surgery is right for them.
No, there isn’t a specific hip replacement lawsuit for manufacturing failures.
However, Exactech is currently being sued for allegedly selling defective hip implants.
As stated earlier, the Exactech lawsuit involves all hip, knee and ankle replacement defects and recalls, not just hip replacements.
Some of the recalled Exactech implants and components are as follows:
The OPTETRAK and OPTETRAK Logic components have been implanted in approximately 60,000 patients in the U.S. since 2004.
The TRULIANT inserts (approx 25,000 units) and VANTAGE Fixed-Bearing Liner Components (1,500 units) are also impacted by the recall.
If you are not sure whether you have received a recalled Exactech knee implant, you should contact your surgeon and check your component’s serial number against Exactech’s provided list.
The most common issue after knee surgery is usually stiffness around the knee joint.
Sometimes this is caused by not following the proper post-operative physical therapy protocol and makes it hard to fully extend or flex the knee.
Additionally, some people may experience problems such as knee implant failure, which involves the knee joint not moving as it should or pain in the surrounding tissues.
Although these problems are relatively rare, it is still important to be aware of them, as they have happened in the case of Exactech.
Most knee implants are designed to last for about 15 to 20 years.
However, this depends on a number of factors, such as the patient’s age and activity level.
In general, younger and more active patients will likely need to replace their implants sooner than older and sedentary patients.
Additionally, some people may develop complications that cause their knee replacement to fail earlier than expected.
After undergoing knee surgery, it is not uncommon to feel some discomfort.
This is because the surgery involves cutting through bone, muscle, and tissue.
In most cases, however, the discomfort is temporary and can be managed with medication.
However, in some cases, the knee replacement may fail.
This means that the joint does not function properly, is painful, and may require revision surgery.
When a knee replacement fails, it is often because the implant has come loose, there is an infection or the bone around the implant has broken, causing pain and disability.
If your Exactech knee implant is failing, you might feel the following symptoms:
Knee replacements are typically considered to be successful procedures, with a high rate of patient satisfaction.
Although uncommon, complications can develop in approximately 1 out of 20 cases.
However, most are minor and treated effectively. Some examples of complications include:
Infections can occur at the incision site or deep within the knee joint after knee surgery.
These are treated with antibiotics, although in some cases, surgery may be necessary to remove the infected tissue.
This is a blood clot that forms in the leg and can be dangerous if it breaks free and travels to the lungs (pulmonary embolism).
Deep vein thrombosis is treated with blood thinners.
Special support stockings, exercise, and anticoagulant medicines can also help eliminate post-operative blood clots.
Sometimes, the bone around the implant does not heal properly, or scar tissue forms that limit joint movement.
Further revision surgery may be needed in these cases to restore mobility and function.
Some patients experience allergic reactions to the bone cement used with knee replacement devices, which can cause difficulty breathing, chest pain, and low blood pressure.
This is a medical emergency that requires immediate treatment.
Sometimes the knee replacement device can become dislocated or move out of place.
This is usually treated with physical therapy and exercises to help strengthen the muscles around the joint.
Over 40% of patients who have undergone total knee surgery still experience pain a year later.
In some cases, this number increases with time, making chronic knee replacement pain more and more common.
If you received Exactech knee implants, particularly from the Optetrak knee implant system range, you might be compensated.
This is especially true if you have experienced side effects or needed revision surgery because of an Exactech recall.
If this is the case, you will likely be eligible to join the Exactech recall lawsuits.
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Here, at Tru Lawsuit Info, we’re committed to helping victims get the justice they deserve.
To do this, we actively work to connect them with attorneys who are experts in litigating cases similar to theirs.
Would you like our help?
Faulty Exactech implants and devices are the subjects of a number of lawsuits, with patients claiming that they have suffered serious complications as a result. If you or someone you love has been affected by an Exactech device, it is important to understand your legal rights.
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