Have you or a loved one suffered serious injury after receiving an Exactech implant?

Hip Replacement Settlement
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In June 2021, Exactech Inc., an orthopedic device manufacturer, issued a Class II Medical Device Recall of its Exactech Connecxion GXL acetabular polyethylene liners used in their hip implants. The unanticipated degradation of a ultra-high molecular weight polyethylene (UHMWPE) component has been found to lead to device failure, bone loss, and increase the need for revision surgeries. According to surgeons “the Exactech Connecxion GXL liner may be prone to a high rate of early failure from wear and severe secondary osteolysis (bone degeneration).

In February 2022, Exactech's knee and hip systems were also recalled due to concerns that the polyethylene liner accelerated bone loss leading to device failure, ultimately requiring corrective surgery. The recalled knee and hip systems were branded as Optetrak, Optetrak Logic, Truliant, and Vantage.

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Did you have an Exactech hip or knee replacement?

Did you receive notice of recall of your hip or knee?
Did you have surgery to revise, remove or replace your hip or knee replacement?

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