A letter was recently sent to surgeons, hospitals, and healthcare professionals announcing the voluntary recall of the Exactech Optetrak Patella implant device. The voluntary Exactech recall concerns Patella lots that were packaged without the ethylene vinyl alcohol (EVOH) layer. Experts advised doctors not to implant these potentially harmful devices packaged in faulty packaging. Medical professionals...
CONTINUE READINGExactech Recall Lawsuit; Connexion GXL Hip Replacement Liner Exactech, a Florida based medical device manufacturer, has issued an FDA Exachtech recall of a number of its medical devices. The recall list includes: Optetrak Optetrak Logic Truliant knee replacement products Vantage ankle replacement products Connexion GXL Hip Liner The hip implant recalls are prompted by the...
CONTINUE READINGMore and more patients are filing Exactech hip replacement recall lawsuits. Exactech is a global medical device company that creates orthopedic implant devices and surgical implants for joint replacement surgeries. In June of 2021, Exactech issued recalls of its knee, hip, and ankle implant systems. The recall cites defective packaging that caused the polyethylene inserts...
CONTINUE READINGTo avoid legal scrutiny in the United States, manufacturer of defective medical implants Exactech is now focusing on ankle replacement surgeries in South America. Manuel Pellegrini, MD, and Giovanni Carcuro, MD, of the Clínica Universidad de los Andes, performed the bilateral ankle procedures in Chile earlier this month. “Many patients worldwide are benefitting from the...
CONTINUE READINGThe 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 normal structure and function in adults. These devices are also...
CONTINUE READINGIn 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 to have the implant revised. In return for covering revision...
CONTINUE READINGIn 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 District of New York State. Since our last post, the...
CONTINUE READINGOn 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 the Multi-District Litigation for the faulty Exactech hip, knee, and...
CONTINUE READINGIn 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 implant, and around 147,700 with an Exactech knee implant. The...
CONTINUE READINGOn 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 for. Although the liners are made of polyethylene, this model...
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