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Exactech® Hip, Knee, Ankle Recall Due to Device Failure Requiring Corrective Surgery

Victims Forced to Suffer a Corrective Surgery After Having a Recalled Exactech® Hip, Knee, or Ankle Implant is Urged to Request a Free, Private Case Evaluation to Potentially Receive Both Justice and Compensation

Those experiencing complications after undergoing certain hip, knee, and ankle implants from Exactech® may be eligible for compensation–types include:

  • Exactech® Connexion GXL acetabular ply liners (used in hip implants)
  • Optetrak® knee & ankle implants
  • Optetrak® Logic knee & ankle implants
  • Truliant® knee & ankle implants
  • Vantage® knee & ankle implants

Limited Time To File A Claim. Check Eligibility Today.

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More about the details and dangers of the Exactech® hip, knee, or ankle implant hardware recall

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Victims who’ve received an Exactech® total knee replacement, total ankle replacement, or total hip replacement may or may not know that some of these medical devices manufactured since 2004 have been recalled for a faulty insert.

Medical device manufacturer Exactech® has issued an urgent recall covering many of its knee, hip, and ankle replacements made since 2004–and not all surgeons have necessarily notified affected patients that they have a recalled knee, ankle or hip implant.

The issue is that the recalled Exactech® hardware devices were manufactured with a “non-conforming” vacuum bag without the technology to ensure quality operation for the expected length of time.

As a result, the premature wear on the plastic components of these medical devices–including bone loss and other dangers or injuries–may even require revision surgery. 

Also, Exactech® issued a recall of some models of liners used for hip implants in the summer of 2021.

Patients with recalled Exactech® devices may be able to make a legal claim for compensation if they suffered injuries, premature wear, or required surgery to fix problems with their knee, ankle, or hip devices.

Here are the injuries and complications common with Exactech® hip, knee, or ankle implant hardware:

  • Revision/replacement/corrective surgery
  • Degeneration of bone (osteolysis)
  • Loosening of device components
  • Dislocation of implant
  • Severe pain
  • Stiffness and reduced mobility

Hundreds of thousands of Exactech® knee, ankle and hip replacements have been put into patients since 2004.

How to know if a victim qualifies for compensation from an Exactech® hip, knee, or ankle implant hardware recall

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Implant hardware manufacturer Exactech® has recalled hundreds of thousands of total knee replacement, total ankle replacement, and total hip replacement systems.

Patients who were made to suffer as a result of this recall may certainly be owed justice in the form of compensation, providing they meet a few criteria with respect to symptoms.

Those who were implanted with an Exactech® knee, ankle or hip device from 2004 and beyond and suffered any of the following symptoms, they may qualify for a free legal case evaluation to determine if they are eligible for compensation:

  • New or worsening pain
  • Inability to bear weight
  • Grinding or other noise
  • Swelling
  • Instability in the knee or ankle
  • Premature wear
  • Osteolysis
  • Revision surgery

The Consumer Justice Action team believes that victims of corrective surgery after a Exactech® hip, knee, or ankle implant hardware recall–and the families that suffered along with them–should be able to address the Exactech® manufacturer and get the compensation and justice they deserve.

Our network of attorneys are ready to support you.

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Depending on the circumstances, the case could be filed for potential compensation

Please seek the advice of a medical professional before making health care decisions. This advertisement is not associated with Exactech®, Optetrak®, Optetrak®, Truliant®, Vantage® or any government agency.

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