Exactech Implant Recall Lawsuit
Exactech recalled over 200,000 knee, hip, and ankle implants due to defective packaging that caused premature wear, device failure, and the need for revision surgery. Lawsuits target Exactech Inc.
Defendant: Exactech, Inc. | MDL 3044 — Eastern District of New York.
Key Facts
Who Qualifies
Individuals who received an Exactech Optetrak, Truliant, Vantage, or Connexion knee, hip, or ankle implant and experienced failure or required revision surgery.
Related Injuries
- Implant failure
- Premature wear and loosening
- Bone loss (osteolysis)
- Pain and swelling at implant site
- Need for revision surgery
- Loss of mobility
- Metal toxicity from wear debris
Settlement Status
No global settlement reached. Cases growing rapidly after the 2022 recall expanded.
Learn More About This Lawsuit
Exactech Implant Recall Lawsuit Overview
Everything you need to know about the Exactech implant recall lawsuit — defective packaging, premature wear, and revision surgery.
Do I Qualify for the Exactech Lawsuit?
Find out if you qualify for the Exactech implant recall lawsuit. Eligibility for knee, hip, and ankle implant claims.
Exactech Lawsuit Settlement Amounts — April 2026 Update
Latest information on Exactech lawsuit settlements, projected case values, and compensation expectations.
Exactech Lawsuit FAQ
Frequently asked questions about the Exactech implant recall lawsuit — eligibility, recall details, and timeline.
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