The U.S. Food and Drug Administration prompted medical-implant manufacturer Exactech to expand its voluntary hip implant recall to all models, not just some of them. Exactech joint replacement devices are used to replace painful, arthritic joints due to osteoarthritis, osteonecrosis, rheumatoid arthritis, and loss of…

In June 2021, Exactech issued recalls of the Exactech Connexion GXL hip liner and the Optetrak and Optetrak Logic knee implants due to premature device failures. To inform implant recipients of their respective device recall, Exactech sent letters to implantees, offering to cover out-of-pocket expenses…

In a recent blog post, we discussed the hearing on September 29th, 2022 to determine where the Exactech multidistrict litigation (MDL) would take place. The primary locations being considered were the Eastern District of Louisiana, the Northern District of Florida, and the Southern or Eastern…

On June 14th, 2022, a motion was filed to consolidate and create a Multi-District Litigation (MDL) for the Exactech cases. A hearing took place at the Thomas F. Eagleton US Courthouse in St. Louis, MO on September 29th, 2022. The hearing was to determine where…

In 2021 Exactech’s Connexion GXL Hip liner and Optetrak/Optetrak Logic Knee implants were recalled leaving more than 200,000 people with faulty devices in their bodies. As of 2019, the FDA reported that there were about 90,000 people in the United States with an Exactech hip…

On June 28, 2021, the FDA issued a recall of the Exactech Connexion GXL Hip Implant liners. This came following reports of high rates of failure around the 3-6 year mark- significantly sooner than the 15 to 20 years they had been marketed to last…

In June of 2021, many orthopedic surgeons received a letter stating Exactech’s polyethylene hip implant had been recalled. The recall was due to the high failure rate of these devices. The implants were marketed to last between 15 to 20 years, but instead were failing…