04/14/2022
In July 2021, Exactech, Inc. issued a Class 2 Device Recall of nearly 90,000 Connexion GXL hip implants due to the risk of polyethylene liner wear which can result in significant pain, bone and tissue damage, component loosening, and the need for revision surgery. If you had a hip replacement after 2007 and have undergone or may require a revision surgery, you may be entitled to compensation. To speak with an experienced product liability attorney about an Exactech hip failure case, call 504-656-6280 or click the button below to learn more information.
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