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Knee Replacement Attorneys in Akron, OH

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Knee Replacement Attorneys in Akron, OH

Knee Replacement Attorneys in Akron, OH

Exactech, known for its commitment to producing top-tier orthopedic devices, faced an unexpected hiccup when a recall for some of their knee and ankle devices was announced. Recalls, while not unheard of in the medical device industry, are a significant concern due to the direct impact on patient health and wellbeing.

For Exactech, the reasons leading up to this recall were multifaceted. Initial reports indicated potential defects in the design and manufacture of certain devices, which were identified through routine inspections and patient complaints. There were also concerns raised from clinical data which suggested potential complications arising post-surgery.

The recall timeline paints a detailed picture. In the early stages, minor complaints and concerns were seemingly sporadic, making it challenging to pinpoint a systemic issue. However, as months progressed, a clearer pattern emerged relating to implant device packaging, compelling health authorities and Exactech themselves to delve deeper. The official expanded recall announcement was a culmination of these investigations. To the company’s credit, it did demonstrate an ability to take ownership of the situation and a first step in making things right for injured patients, including those in Akron, Ohio.

Affected Exactech Products

The recall encompassed a range of products, each designed to enhance mobility and alleviate pain for patients with joint issues. Among the most notable were:

  • Optetrak Knee System: A flagship product, the Optetrak system was designed for patients undergoing total knee replacements. Concerns arose due to reports of premature wear and potential misalignment post-surgery.
  • Vantage Ankle Solutions: Touted as a breakthrough in ankle joint replacements, the Vantage system faced scrutiny after some patients reported reduced mobility and discomfort months after their procedures.

Alongside these primary products, several other lesser-known knee and ankle devices were highlighted. Each had its own set of identified defects, ranging from manufacturing inconsistencies to design flaws that might compromise the intended function and longevity of the device.

Risks and Complications

The fallout from a medical device recall isn’t merely logistical; it bears a heavy human cost. Patients equipped with the affected Exactech devices reported a myriad of complications. For some, it was a persistent pain, sharper and more intense than what they’d experienced before the surgery. Others noted swelling, reduced mobility or even the alarming sensation of their implant moving or clicking.

Such complications can drastically affect a patient’s quality of life. Simple tasks become arduous, and the emotional toll of revision surgery becomes a real possibility for many. Instances of device fractures, post-surgical infections or inflammatory reactions have been documented. These severe cases sometimes require emergency medical interventions, further surgeries and prolonged rehabilitation.

What to Do if You Have an Exactech Device

  • Consultation: Schedule an appointment with your orthopedic surgeon or healthcare provider. They can confirm whether the implanted device is among those recalled.
  • Monitor Symptoms: Pay attention to any unusual symptoms such as increased pain, swelling, or reduced mobility. Simply having a recalled device does not necessarily mean you will experience complications.
  • Medical Records: Keep a comprehensive record of your medical history, surgical reports and any post-operative complications. This information can be invaluable for both medical and legal consultations.
  • Stay Informed: Regularly check updates from both Exactech and relevant health authorities. Staying updated can provide guidance on managing potential risks.

Legal Rights and Compensation After an Implant Injury

While Exactech’s recall was the right call for the company to make, affected patients who have suffered injuries and required revision surgeries still have rights to consider. A recalled medical device can lead to additional medical bills, loss of wages due to recovery periods and pain and suffering. Patients may be entitled to compensation for such damages.

Historically, medical device recalls have led to substantial settlements or verdicts in favor of the affected patients. Legal action can ensure that corporations remain vigilant about patient safety and can provide financial relief for affected individuals.

If you or a loved one has an implanted Exactech device, it might be prudent to consult with our Knee Replacement Attorneys in Akron, OH at the Buckeye Law Group. They can offer insights into your potential claim, guide you through the legal maze, and ensure your rights are upheld. Our dedicated Knee Replacement Attorneys in Akron, OH are here to help you navigate your situation and seek the compensation you deserve.

Don’t hesitate to reach out to our Knee Replacement Attorneys in Akron, OH for a consultation. Your health and legal rights are important to us, and we are committed to assisting you in your recovery journey.

 

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Are You an Akron Patient Affected by a Recalled Ankle or Knee Implant?

The Exactech recall serves as a crucial reminder of the balance between medical innovation and patient safety. While the company’s proactive steps are commendable, affected patients must remain informed, vigilant and proactive in seeking both medical and legal advice. Don’t hesitate to call our team at 1-800-411-PAIN for a free case evaluation to discuss your situation.