Joint replacement surgeries can significantly improve a patient’s quality of life. However, the use of faulty prosthetics can cause severe complications, leading to lifelong pain and suffering.
In recent years, Exactech Replacement Recalls have become a significant concern in the medical community, affecting patients who have had knee, hip, and ankle prosthetics installed. Let’s discuss the impact of Exactech Replacement Recalls on patients, types of lawsuits, safety concerns, signs of defective replacements, legal implications, and compensation for victims.
Introduction to Exactech Replacement Recalls
Exactech is a medical device company that produces and distributes orthopedic implants for joint replacement surgeries.
In August 2020, Exactech Inc., a Florida-based medical device manufacturer, issued a voluntary recall of the OPTETRAK knee / ankle implant system. The recall was issued due to a defect in the device’s tibial component, which can cause several serious side effects, including pain, swelling, and difficulty walking.
Patients who have received a hip, knee, or ankle implant since 2004 that was manufactured by medical device company Exactech, please contact us and your physician for guidance on what you need to know and do to prevent further injury and to make an Exactech implant recall claim.
While their products have been successful in the past, they have also faced controversies regarding their safety and effectiveness. In recent years, patients who have received Exactech knee, hip, and ankle units have reported complications that led to the recall of certain products, including the Optetrak Knee Replacement System, the Alteon Cup System, and the Novation Crown Cup System.
Understanding the Impact of Exactech Replacement Recalls on Knee, Hip, and Ankle Prosthetics
The impact of Exactech Replacement Recalls on patients who have received knee, hip, and ankle prosthetics can be devastating. Patients who have received defective replacements may experience severe pain, limited mobility, and other complications that can affect their daily lives. In some cases, these complications may require revision surgeries, which can be risky and expensive. Patients who have received Exactech knee, hip, and ankle prosthetics should be aware of the potential risks and complications associated with these products.
Exactech Recall Lawsuits, Class Action or MDL Status?
There are two types of Exactech recall lawsuits: individual lawsuits and class-action lawsuits. Individual lawsuits are filed by patients who have experienced complications due to defective Exactech prosthetics. These lawsuits seek compensation for medical expenses, lost wages, and pain and suffering.
The Exactech knee recall lawsuit is a multi-district litigation (MDL) that has been filed against Exactech Inc. by former recipients of the Connexion GXL implant system. The lawsuit alleges that Exactech failed to adequately warn consumers of the risks associated with the defective device, and seeks financial compensation for the medical expenses and emotional suffering caused by the defect. The Exactech recall lawsuit includes both individual and class action claims, with a wide range of plaintiffs from all over the country.
Class-action lawsuits are filed on behalf of a group of patients who have received the same defective product. These lawsuits seek compensation for damages suffered by all members of the class. As of this writing there is no class action lawsuit for these problematic Exactech prosthetics.
Safety Concerns Associated with Exactech Replacement Recalls
The safety concerns associated with Exactech Replacement Recalls are related to the design and manufacturing of the products. Patients who have received faulty prosthetics may experience mechanical failure, which can cause the device to dislocate or break.
If you are experiencing any of the following symptoms, your Exactech implant may be one of the recalled devices and could have failed due to degradation or deterioration:
- Chronic or worsening pain in hip, knee or ankle
- Feeling of loosing or grinding
- Instability or limited mobility
- Osteolysis, or degeneration of bone tissue
- Device failure or malfunction
- Revision surgery due to any of the above
These complications can lead to severe pain, limited mobility, and other health problems. In some cases, patients may require revision surgeries to correct these issues.
Signs and Symptoms of a Defective Exactech Replacement
Patients who have received Exactech knee, hip, and ankle prosthetics should be aware of the signs and symptoms of a defective replacement.
Exactech Knee System Names and Models Recalled:
- OPTETRAK® Unicondylar Tibial Components
- All-polyethylene CR Tibial Components
- All-polyethylene PS Tibial Components
- B-Series Ps Tibial Insert
- CC Tibial Inserts
- CR Tibial Inserts
- CR Slope Tibial Inserts
- TRULIANT® CR Tibial Inserts
- TRULIANT® CR Slope Tibial Inserts
These may include severe pain, limited mobility, instability, and difficulty walking or standing. Patients who experience any of these symptoms should contact their physician immediately to discuss their options.
What to Do if You Have an Exactech Replacement
If you have received an Exactech knee, hip, or ankle prosthetic, it is essential to monitor your symptoms and report any issues to your physician. If you experience severe pain, limited mobility, or other complications, you may need to undergo revision surgery to correct the problem. It is also important to keep records of your medical treatment and any expenses incurred as a result of your complications.
Legal Implications of Exactech Replacement Recalls
Exactech Replacement Recalls have significant legal implications for patients who have received faulty prosthetics. Patients who have experienced complications may be entitled to compensation for medical expenses, lost wages, and pain and suffering. In some cases, patients may also be entitled to punitive damages, which are intended to punish the manufacturer for their negligence.
How to File a Lawsuit Against Exactech
Patients who have received Exactech knee, hip, or ankle prosthetics and have experienced complications may be eligible to file a lawsuit against the manufacturer. To file a lawsuit, patients must first consult with our attorneys, we specialize in medical device litigation. Our attorneys will review your medical records and determine the best course of action.
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Compensation for Exactech Replacement Recall Victims
Victims of Exactech Replacement Recalls may be entitled to compensation for a variety of damages, including medical expenses, lost wages, and pain and suffering. In some cases, victims may also be entitled to punitive damages, which are intended to punish the manufacturer for their negligence. The amount of compensation awarded will depend on the severity of the patient’s complications and the extent of their damages.
Begin the Exactech Claims Process
The use of faulty prosthetics can cause severe complications, leading to lifelong pain and suffering. Patients who have received Exactech knee, hip, and ankle prosthetics should be aware of the potential risks and complications associated with these products.
If you have experienced premature wear of any of these Exactech Hip, Knee or Ankle products contact us today for a free injury case review at 1-800-631-5656 or use the claim form on the right side of this page, we intend to hold the manufacturer responsible to the failure of it’s medical devices.
If you have received an Exactech replacement and have experienced complications, it is essential to contact our attorneys, we specialize in medical device litigation and are available to discuss your legal options. Act today as there are statute of limitations that apply.
Understanding the Impact of Exactech Replacement Recalls on Knee, Hip and Ankle Prosthetics Page Updated on March 24, 2023.