Nadrich Accident Injury Lawyers is representing those who have suffered failures of defective Exactech knee implants. We can help you recover financial compensation for medical bills, lost wages, lost earning capacity, pain, suffering and more.
We have been representing victims of defective medical devices such as Exactech implants since 1990. We have recovered over $750 million for our clients. Our extensive experience in handling cases like yours will allow us to recover the most financial compensation possible for you.
We will handle your Exactech implant case on a contingency fee basis. This means that the only fee you will ever owe us is a percentage of whatever compensation we recover for you. We don’t charge upfront fees or out-of-pocket fees. You won’t owe us anything until and unless we obtain a recovery.
We get our clients who can’t afford medical treatment to doctors who treat them on a lien. This means you won’t be charged for treatment until your case ends. We get great results for our clients and that’s why doctors do this for our clients.
Call us today for a free consultation if you or a loved one suffered the failure of a defective Exactech knee device. You can also text us from this page or fill out this page’s free case evaluation form.
Who Can File an Exactech Knee Replacement Lawsuit?
We are actively seeking cases involving those who have had knee replacement surgery after 2004 then experienced the failure of one of the following defective Exactech implants:
- Exactech Optetrak
- Exactech Optetrak Logic
- Exactech Truliant
When these devices fail, they can cause pain and possibly a need for revision surgery. If you’ve undergone revision surgery, have been told you need a revision surgery, or are simply experiencing pain after having one of the above devices implanted, call us today for a free consultation.
Compensation Available in an Exactech Implant Lawsuit
Those who file Exactech lawsuits may be able to recover financial compensation for:
Medical Bills
You may already be facing medical bills due to the failure of your knee implant. You might have seen a doctor due to the pain you’re feeling. You may have already had a revision surgery. The complications you’ve experienced could also cause you to need treatment in the future. We will seek to recover compensation for all past and future medical expenses which are related to your recalled Exactech knee.
Lost Wages
Those injured by knee replacement devices may be injured so badly that they’re not able to work for a period of time. Those injured by an Exactech knee replacement system may also need to take time off from work in order to have their injuries treated. We can help you recover financial compensation for any wages you’re unable to earn because of your failed implant.
Loss of Earning Capacity
Your implant failure could have caused you to suffer a disability. This may have led to a reduction or loss of your earning capacity. When we file an Exactech lawsuit on your behalf, we will seek compensation for any loss or reduction of your earning capacity caused by your device failure.
Pain and Suffering
The failure of a device subject to an Exactech implant recall may have caused you to experience physical pain and mental suffering. We have the experience and know-how to accurately calculate the financial value of your pain and suffering and make sure you’re fairly compensated for it.
Wrongful Death
Unfortunately, death is always a risk any time a surgery involving anesthesia is needed. If you have lost a loved one due to the failure of an Exactech knee replacement, we can get you compensated for your suffering and grieving. We can also get you compensated for your loved one’s pain, suffering, medical bills, funeral costs and burial costs. We can also get you compensated for the loss of your loved one’s household services, income, love and companionship.
How Much Compensation Can I Expect?
You might be wondering how much compensation you can expect if you file a lawsuit. Estimated settlements for Exactech knee replacement lawsuits range from between $100,000 to $300,000, and the primary determining factor is the injury severity.
Claims for compensation might include reimbursement for lost income, medical bills, and pain and suffering. It’s vital to understand that the $100,000 to $300,000 figure given is just an estimate and that the actual amount of compensation can vary based upon the specifics of your individual case. A lawyer with experience handling these lawsuits can help you navigate the legal process and maximize your financial compensation.
Estimating Your Case’s Value
In terms of estimating Exactech knee replacement lawsuits’ value, numerous factors are considered. It’s projected that settlements will range from $100,000 to $300,000, but the value could vary depending on the specifics of the case. The value of your lawsuit may vary based upon:
- How long it took for you implant to fail – early failures often result in more compensation
- Your employment status and age
- The specific pain and harms incurred
- How much medical treatment you need
Exactech knee implant victims might qualify for financial compensation for lost income, pain, suffering and medical bills which result from the failure of an implant. Attorneys who deeply understand specifics regarding the recalled devices can maximize your compensation by leveraging info like the defective packaging and high failure rates which are documented by an FDA database.
Exactech Recall
Exactech hip, ankle, knee and shoulder replacement devices have been recalled. They have been recalled because they may fail prematurely. Early failure can happen because their parts were packaged improperly prior to implantation.
The parts in question were supposed to be packed in vacuum bags containing a layer of ethylene vinyl alcohol (EVOH). This EVOH layer makes the bags more resistant to oxygen. However, this layer was missing from the bags that the parts were packaged in.
These defective bags can cause excessive oxygen to reach the parts before implantation. This can cause the parts to oxidize and wear out quickly or become damaged after implantation.
The following Exactech knee replacement parts have been recalled:
- Optetrak All-polyethylene PS Tibial Components
- Optetrak All-polyethylene CR Tibial Components
- Optetrak CR Slope Tibial Inserts
- Optetrak CR Tibial Inserts
- Optetrak HI-FLEX PS Tibial Inserts
- Optetrak PS Tibial Inserts
- Optetrak Logic CR Slope Tibial Inserts
- Optetrak Logic CR Tibial Inserts
- Optetrak Logic PS Tibial Inserts
- Optetrak Logic CRC Tibial Inserts
- Optetrak Logic CC Tibial Inserts
- Optetrak Logic PSC Tibial Inserts
- Truliant CR Slope Tibial Inserts
- Truliant CR Tibial Inserts
- Truliant PS Tibial Inserts
- Truliant CRC Tibial Inserts
- Truliant PSC Tibial Inserts
Reports to the MAUDE database mentioned premature failures of Exactech implants as early as 2012. However, Exactech didn’t begin recalling devices until August 2021.
Exactech knew or should have known that its devices were failing prematurely due to the defective vacuum bags. Let us help you hold Exactech accountable for their failure to remove dangerous products from the marketplace. Call us today for a free consultation.
Issues With Optetrak Knee Implants
Optetrak knee implants were approved via the FDA’s abbreviated 501(k) clearance process. This means the device was not subject to a full review by the FDA. Optetrak implants were successful for a decade after they were initially released in 1994. However, from 2004 on, the implant system saw abnormally high rates of failure.
In 2012, “poor results” were highlighted by Orthopedics and Traumatology. These results involved Optetrak knee implants and it was suggested the results were due to a flawed design.
In 2016, Optetrak implants were identified by the Australian Registry as having a revision rate which was higher than expected. The implants were found to have the highest failure rates of any knee implants at five, seven and ten years.
Exactech knew about these high failure rates, as they were receiving a deluge of incoming reports regarding failures of implants from around the United States starting in 2012. It was indicated by reports to the MAUDE database that revisions were occurring for multiple reasons. These reports of early onset failure represent the higher rate of incidents which Exactech had become aware of. The MAUDE database contains so many complaints regarding Optetrak devices that a single search can’t show them all since it maxes out.
Lawsuits against Exactech were sparked by reports of excessively high rates of failure regarding the Optetrak implants. These lawsuits, filed by patients who saw their implants fail prematurely, alleged that the devices had a high failure rate due to design defects.
Exactech’s response to the situation was to issue a “silent” recall which involved them gradually phasing out the design of the product without making an announcement. However, when Exactech changed the product’s design, the high failure rates didn’t decrease, and this led to Exactech discovering the issue with the packaging which was causing components to become oxidized and malfunction prematurely.
Exactech’s Sales Reps Knew of the Problems
Exactech’s general practice, as with the majority of implant makers, is to make sure that authorized sales representatives are present when surgeries are done to provide components of implants to surgeons. This practice ensures hospitals don’t have the responsibility for keeping all possible components and sizes which might be needed for surgeries in stock. Sales reps for Exactech were present for original implant surgeries as well as revision surgeries.
Sales reps for Exactech observed plenty of cases of Optetrak devices failing prematurely. They saw clear evidence that the plastic inserts were prematurely degrading, and surgeons often noted this as well. These sales representatives would often take components from surgeons and return them to Exactech for analysis and inspection.
These sales reps had a duty to report their findings to Exactech’s medical and engineering departments. These departments had a duty to investigate the findings, analyze the components, and thoroughly and honestly report their findings to surgeons and the FDA. This failed to happen. The sales reps reported the problems to Exactech, but the company continued promoting and selling their implants without warning the FDA, patients or surgeons that evidence was growing that the devices were prone to failing prematurely.
Despite knowing about the issues in 2012, the company never changed its labeling, product inserts or marketing materials to accurately and adequately warn physicians and patients about the risks associated with the devices. It wasn’t until August of 2021 that the company finally recalled its Optetrak devices as well as other devices.
How Do I File an Exactech Lawsuit?
The process of civil litigation is extremely time-consuming. It requires a lot of attention to detail and knowledge regarding legal jargon.
Those coping with pain, complications and trauma from their injuries may find the legal process overwhelming.
With the assistance of our lawyers, you can begin to collect evidence which will strengthen your case.
Our legal team can help you collect evidence and assess the damages you’ve suffered.
Hiring an Exactech Knee Replacement Lawyer
It will be very helpful for your case for you to hire an attorney who has extensive knowledge regarding the recalled Exactech devices.
Our lawyers can simplify the lawsuit process and work along with you in order to make your claim stronger.
It’s vital for you to hire a lawyer with a history of success. We have been handling defective medical device cases successfully for over three decades.
If you have been injured by a defective Exactech knee replacement, call one of our lawyers as quickly as possible.
It’s difficult to recover from medical implant failures. You don’t have to get through this difficult time alone. Call us today to discuss your legal options as well as how our team can help you.
Collecting Evidence
It is crucial to collect evidence to build a strong claim.
Evidence to collect includes records and documentation relating to your injuries and defective device.
Evidence you may need to gather includes:
- Medical records
- Witness testimony
- Doctor’s notes
- Employment records
- Videos and photos
- Other evidence that proves you used an Exactech implant and were injured by it
Call a lawyer with experience handling defective medical device claims for insight regarding what evidence needs to be gathered to build a convincing case.
Calculating Damages
Damages are your financial losses related to the injuries you suffered due to your defective implant.
Our legal team will help you with calculating damages.
Damages in your lawsuit might include:
- Past and future medical bills
- Lost wages
- Lost earning ability
- Loss of quality of life
- Permanent disability
- Emotional damages
- Pain and suffering
- Other compensatory damages
- Punitive damages
It’s important to calculate these damages. It helps your attorney better understand how your defective implant impacted you and how much compensation you’re entitled to.
Mitigating Your Injuries
It’s also important to mitigate your injuries.
Mitigation involves trying to lessen your injuries’ impact and the costs related to them.
Properly mitigating your injuries includes:
- Getting your injuries officially diagnosed
- Seeking treatment for your injuries
- Following the orders of your doctors
- Talking about revision surgery if your medical providers say it’s safe and beneficial
- Doing whatever you can to minimize your injuries’ extent
It’s very important to mitigate your injuries if you want to build an honest, strong claim.
If you take too long to call a lawyer and your case’s statute of limitations expires, you could lose the right to seek compensation for your injuries.
Call us today and allow us to help you move towards healing.
What Should I Do if My Exactech Knee Replacement Has Been Recalled?
If you have an Exactech knee implant which has been affected by a recall, you should contact your doctor, especially if you’re experiencing:
- New or worsening pain
- Inability to bear weight
- Grinding or other noise
- Swelling
- Joint instability
You should contact your surgeon if you’re unsure whether you have one of the implants that have been recalled. The surgeon who did your knee replacement surgery may contact you to make sure your implant is working properly and order X-rays if they suspect you have a failed implant.
Surgery is not recommended by Exactech for people who aren’t having pain or other problems like trouble walking. Exactech said patients and doctors should work together to make decisions about exchanging or removing devices. Doctors should explain the risks and benefits of every treatment option to patients.
On its website, Exactech explains the process for patients with defective implants to submit claims and receive financial compensation for implant-related expenses. However, our Exactech recall lawyers would like to let you know that any patients who file claims directly with Exactech might waive their rights to sue Exactech.
Patients who need revision surgery because of Exactech’s defective implants might be able to file a lawsuit against Exactech and seek financial compensation, including compensation for lost wages, medical bills, pain, suffering, and more.
Such a lawsuit may end up providing you with far more compensation than filing a claim directly with Exactech would. Because of this, you should speak to an Exactech knee recall attorney today before agreeing to a settlement with Exactech. You don’t want to forfeit your right to financial compensation in an Exactech implant lawsuit.
How Much Do Exactech Lawyers Cost?
Our attorneys represent clients on a contingency, meaning we will only be paid if you get paid. No out-of-pocket or upfront costs will be charged for you to work with our attorneys.
Is There a Time Limit to File a Lawsuit?
Unfortunately, there is a time limit for you to file an Exactech knee implant lawsuit because of state laws known as statutes of limitations.
The time limit varies from state to state. Therefore, it’s vital to contact a lawyer as quickly as you can once you begin experiencing Exactech implant side effects.
If you wait too long, you will lose your opportunity to file a lawsuit over your injuries.
Call us today to learn about your legal options and get the legal process moving.
Loose Knee Replacement Symptoms
It is unfortunate that it isn’t uncommon for patients to experience symptoms of a loose knee replacement after undergoing knee replacement surgery. Knee replacements’ annual failure rate is about 0.5 percent to 1 percent.
Symptoms of a failed knee replacement might include:
- Instability
- Decreased joint function
- Swelling
- Stiffness
- Pain
Persistent swelling and pain might indicate loosening of a knee replacement or infection. If you have an Exactech knee replacement and you have experienced any side effects, you may qualify to file a lawsuit.
Call us today for a free consultation.
Was My Implant Recalled?
If your Exactech knee replacement implant was implanted between 2004 and August 2021, then it is virtually certain that your implant was recalled. The recall covered all total knee replacements by Exactech which were made at any time after 2004.
Did Exactech Make My Implant?
A lot of patients who have joint replacements implanted don’t know the brand of their implant. If you have undergone knee replacement surgery but aren’t aware if your implant was made by Exactech or not, you are going to need to request this information from your orthopedic doctor, or ask for your medical records regarding your surgery in order to determine the manufacturer of your implant.
Exactech Knee Replacement Lawsuit Updates
October 30, 2024 Update
Exactech has filed for bankruptcy amid increasing liabilities and legal costs which stem from numerous recalls over defective implants issued in recent years.
In 2021 and 2022, a series of recalls by Exactech got announced due to certain components being stored in vacuum sealed bags missing an oxygen protection layer, allowing oxygen to get to components prior to them being implanted.
This led to the implants degrading prematurely, which increases the risk of device failure and revision surgery.
Over 2,500 lawsuits have been filed since these recalls.
The manufacturer hopes the bankruptcy will help to resolve any outstanding liability and let the company restructure.
Exactech claims that selling the company and restructuring it will lead to a capital infusion which will allow it to pay plaintiffs in the Exactech litigation.
October 3, 2024 Update
The Exactech MDL saw around 50 cases get added to it during the summer, and now involves 1,670 pending cases.
September 5, 2024 Update
The summer has seen around 50 cases added to the Exactech MDL, which now contains 1,670 cases which are pending.
In other news, trial dates have now been set for the initial two bellwether trials in the MDL. July 6, 2025 will see the start of Gayle Tarloff's trial. September 29, 2025 will see the start of Geraldine Larson's trial.
We predict and hope that the bellwether trials will never take place due to a global settlement happening in 2025.
August 21, 2024 Update
The judge overseeing the Exactech MDL approved an update to the pretrial schedule which the parties proposed. The update delays the beginning of the first two trials by several weeks in order to allow for more time for discovery.
A bit more time has been called for in order to prepare these claims to be tried before juries than originally provided. The start of the first trial has been pushed back from June 2025 to July 2025. The second trial, which was expected to start in August 2025, is now expected to begin in September 2025.
An order issued previously had set the dates for the first two trials for June and August 2025. However, this schedule was questioned after an Exactech recall happened in April 2024. This recall affected components used by plaintiffs in the bellwether trials.
On August 16, defendants and plaintiffs sent a letter to the judge which jointly proposed an update to the pretrial schedule in order to resolve any issues resulting from the new recall. The proposed schedule was approved by the judge.
August 12, 2024 Update
The judge presiding over the Exactech MDL agreed on a joint request regarding changing early test trials’ order. The trials are set to start in June 2025 and lawyers who are involved in other claims will closely watch them as they will help in determining how juries might respond to testimony and evidence which will get repeated during litigation.
The schedule changes got proposed as a response to an Exactech recall which was announced in April of 2024 which impacted some knee components which are at issue regarding two of the first bellwether trials. The schedule shuffling will give parties more time in order to complete discovery and won’t delay the first trial dates’ beginning.
Over 1,600 lawsuits have been filed regarding issues with defective knee, ankle and hip components which were first removed from the market in 2022 because of faulty vacuum-sealed bags.
The lawsuits claim the faulty bags allowed components to be exposed to oxygen before being placed in bodies, causing the components to degrade as well as prematurely fail, sometimes leading to a need for component removal surgery.
June 3, 2024 Update
Starting dates have been announced for the third and fourth bellwether trials in the Exactech MDL. The bellwether trials are part of an early series of test trials which are intended to gauge how juries might respond to certain testimony and evidence which will end up being repeated through over 1,200 claims brought over allegations that early device failure risk was increased by defective packaging.
The claims allege that vacuum-sealed bags which were “out-of-specification” allowed oxygen to reach artificial joints which were implanted in people, increasing the risk that the devices degrade and fail prematurely, necessitating surgery to remove and replace the devices.
Last month it was announced that the initial two bellwether trials will start in June and August 2025. On May 22, it was announced the third and fourth bellwether cases will begin in October 2025 and then January 2026.
In other news, 42 cases were added to the Exactech MDL in May, bringing the total number of cases to over 1,500.
May 6, 2024 Update
61 cases were added to the Exactech multidistrict litigation in April, bringing the total number of pending cases to 1,462.
April 30, 2024 Update
Trial dates have been set by the MDL judge. The first bellwether trial, involving Gayle Tarloff, will begin in June 2025. The second bellwether trial, involving Geraldine Larson, will begin in August 2025. The third bellwether trial, involving Dana Kessler Kramer, will begin in 2025 on a date to be determined.
For the fourth trial, parties will confer and agree upon a pick from plaintiffs’ lawyers by May 3.
The Tarloff case involves a New York woman who received an Optetrak Logic implant in 2016. The woman claims that she needed a revision surgery seven years later due to weakness, discomfort, stiffness and pain.
While it is frustrating that these trial dates are over one year away, we expect and hope that most of the lawsuits in the MDL will end up being settled prior to the Tarloff trial.
April 16, 2024 Update
The private meeting which the defendants had requested of the judge overseeing the Exactech MDL last month has been denied by the judge.
The request for the meeting had included asking for deadlines to be pushed back, which the plaintiffs pushed back against. The judge seemingly agreed with the plaintiffs’ objections to pushing back deadlines.
April 4, 2024 Update
147 cases have been added to the Exactech MDL in March, bringing the total number of cases pending to 1,401.
March 31, 2024 Update
Lawyers for Exactech are requesting a private meeting to be held with the judge overseeing the Exactech recall MDL, asking the court to give priority to global settlement negotiations instead of efforts regarding the preparation of claims for trials.
Exactech’s lawyers noted that the cost of the litigation has been substantial for Exactech as well as the plaintiffs, encouraging the court to discuss possible global litigation mediation before both parties incur more expenses in litigation.
March 23, 2024 Update
The FDA sent Exactech a warning letter regarding repeated issues with joint replacement implants’ packaging which led to numerous massive recalls as well as hundreds of lawsuits alleging device failures.
The letter indicates Exactech did not establish the proper procedures in order to prevent and correct packaging issues.
The FDA noted that packaging errors have caused devices to degrade on shelves, leading to:
- Joint subluxation
- Instability
- Subsidence
- Range of motion loss
- Pain
- Migration
- Total joint dislocation
Exactech is facing over 1,100 lawsuits alleging its joint implants prematurely failed due to manufacturing defects.
March 17, 2024 Update
A court has ruled that plaintiffs have failed in proving that private equity owner TPG Inc. sufficiently controlled Exactech in order to be held liable for any injuries. While TPG has influence over the business strategy of Exactech, the court did not find any evidence that they had complete control.
Product recall delays and insurance coverage delays were also deemed part and parcel of typical corporate operations.
Claims against TPG have thus been dismissed by the court.
This is probably not a big deal, but it would have been nice for plaintiffs to have an additional big pocket for contributions towards settlements.
March 9, 2024 Update
February saw 75 new cases added to the Exactech MDL, bringing the total number of pending cases to 1,244.
February 19, 2024 Update
79 new Exactech cases were added to the MDL in January, bring the total number of cases which are pending in the MDL to 1,169.
January 31, 2024 Update
The judge overseeing the Exactech knee, ankle and hip MDL has called for 12 lawsuits regarding knee replacements to be selected as bellwether trials, which will be tried in mid-2025. The lawsuits will involve complications with Exactech’s Truliant, Logic and Optetrak knee implants. Eight of the cases will be randomly selected, and the plaintiffs and defendants will each pick two more cases.
Exactech is facing over 1,100 lawsuits in federal court alleging that manufacturing defects led to joint implants failing prematurely.
December 1, 2023 Update
In October, the multidistrict litigation ordered that the company Exactech needs to produce around 35,000 documents since it was discovered that the documents were withheld inappropriately during discovery. The company already produced the documents, but in October Exactech filed a motion which asked the judge to essentially rescind the finding that the documents were withheld inappropriately. This is because lawyers for Exactech are complaining about plaintiff lawyers using the finding in state court. Exactech also complained in the filed motion regarding how producing the documents will cost around $38,000. The company likely spent up to 20 times as much in attorney fees disputing the documents being discoverable. The company is now spending yet more money filing this motion to reconsider.
November 1, 2023 Update
A video status conference regarding a class action lawsuit over the Exactech devices is now scheduled for 12-20-23. Some plaintiffs would prefer this litigation be moving more quickly.
184 cases were added to the MDL in the past month. There are now 842 cases pending. The total in June was only 391. The MDL has grown a lot.
Exactech MDL parties submitted to the judge a joint status report before a status conference. 984 cases are pending in the MDL according to the report. 811 of the cases involve knee implants, 164 involve hip implants, and 9 involve ankle implants. 327 more cases are pending in state courts in Florida, consisting of 233 knee cases and 90 hip cases.
Exactech plaintiffs’ lead counsel sent the court a letter in September which explained that a major dispute regarding discovery may be developing. The letter claims that Exactech refuses to produce documents which were requested during discovery. This includes documents which relate to prior litigation regarding Exactech, as well as documents which involve action that European regulators took involving Exactech implants. The defense team for Exactech now contends the documents aren’t relevant to current litigation, even though documents like these are extremely typical of documents produced in MDLs regarding mass torts.
October 1, 2023 Update
Exactech is facing a class action MDL. They are also facing a False Claims Act lawsuit which alleges Exactech committed fraud against the federal government when they sold defective knee implants to VA, Medicaid and Medicare. In this case, a judge ruled recently that the government probably would have denied payment to the company if they knew the implants had a high failure rate. The ruling is possibly significant regarding the plaintiffs making the argument in class action lawsuits.
All parties are looking for relif from the quickly moving bellwether trial and scheduling order. A joint brief filed by Exactech lawyers included a hearing transcription where a defense lawyer is talking about Exactech being a small company and how scheduling orders should consider this. This is puzzling, since Exactech’s market cap is estimated to between $4 billion and $6 billion.
The Exactech MDL has built momentum. 658 cases are now pending in the MDL – 267 new cases were moved into the MDL through the summer. The MDL’s size essentially doubled since Memorial Day.
September 1, 2023 Update
The Exactech litigation was the busiest MDL for a mass tort in America in July. Most MDLs saw record low case volumes filed in July, but the Exactech MDL almost doubled in size in July. 567 cases are now pending in the MDL. Only 136 cases were pending only two months ago. Florida state courts have another 272 cases pending.
822 claims are pending in the federal Exactech implant MDL. 665 of the cases are knee implant lawsuits. There are 146 hip implant lawsuits and 10 ankle implant lawsuits.
Exactech’s primary American office is in Florida, so victims are allowed to sue in Florida state courts. There are 272 lawsuits ongoing in state court, including 191 knee lawsuits, 77 hip lawsuits and 4 ankle lawsuits. 14 cases were filed in Illinois. 23 more claims were filed in other state courts.
In July, parties in the Exactech MDL submitted a plan for a proposed bellwether trial. There are also 80 Exactech lawsuits which are proceeding in Florida state court.
The bellwether plan which was proposed would look to coordinate federal and state MDLs by calling for bellwether trials in federal court focusing on cases which involve Exactech knee devices.
The Florida MDL would see bellwether trials held in cases which involve hip implants. The bellwether trials in the federal MDL would end up being selected from 24 knee implant lawsuits.
Experienced Representation
We have been representing those injured by defective medical devices since the founding of our firm in 1990. In that time, we have recovered in excess of $750 million for injury victims.
We have vast experience handling cases just like yours. We know how to prove that our clients’ injuries were caused by the negligence of someone else. We know how to collect evidence and use it to put together a strong, convincing case. We have the experience and resources to recover the maximum possible compensation in your case.
Call us today for a free consultation if you or a loved one has experienced the premature failure of an Exactech knee replacement. You may qualify for financial compensation in a lawsuit against Exactech. Remember: you will not owe us any fee until and unless we win your case. Call us today.
