THe FDA has updated its Exactech implant warning with recommendations for doctors and patients, detailing when revision surgery might be necessary.
An Exactech knee implant lawsuit alleges a polyethylene tibial insert, later recalled due to defective packaging, failed, resulting in the need for revision surgery.
Parties have proposed a "Science Day" in mid-April to educate the court on the scientific principles behind Exactech implant failure risks.
A Exactech Truliant knee system lawsuit claims defective packaging led to device failure and the need for revision surgery.
A woman who suffered an Exactech total knee failure says the manufacturer knew about the problems with the implant for years without providing proper warnings.
A federal judge has appointed 27 Exactech recall lawyers to leadership positions in the consolidated federal litigation.
A lawsuit filed over a failed Connexion GXL hip liner claims a hip implant designed to last 20 years failed after only four, resulting in the need for revision surgery.
An Exactech Logic knee lawsuit filed by a New York woman indicates her tibial insert failed, only to be replaced with another defective insert that was later recalled.
An Optetrak Total Knee System lawsuit claims Exactech knew the device had high failure rates due to the risk of complications, but delayed recalling the devices.
Exactech recall attorneys will meet with a federal judge for the first time to begin structuring the pretrial proceedings for the joint replacement litigation.
