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1 MINUTE SURVEY FORM
https://survey.medicalclaimcenter.com/project/3
3 MINUTE SURVEY FORM
https://survey.medicalclaimcenter.com/
One of the most significant lawsuits against Exactech was filed in 2018 by a group of patients who had received Exactech Optetrak knee implants. The plaintiffs claimed that the knee implants were defectively designed and caused them to suffer severe injuries, including pain, instability, and the need for revision surgery. The lawsuit alleged that Exactech knew about the defects in its knee implants but failed to warn patients or the medical community about the risks associated with the devices. The case was consolidated into a multidistrict litigation (MDL) in the United States District Court for the Northern District of Indiana. In 2020, the court approved a $30 million settlement agreement between Exactech and the plaintiffs. The settlement resolved approximately 1,900 claims and provided compensation to patients who had undergone revision surgery or had their knee implants removed due to complications. The settlement also established a program to provide additional medical monitoring and care to patients who had received the Optetrak knee implants. In addition to the knee implant lawsuit, Exactech has faced legal action related to its ankle and hip replacement products. In 2020, a group of patients filed a class-action lawsuit against Exactech and its distributor, alleging that the Exactech Equinoxe Reverse Shoulder System was defectively designed and caused them to suffer severe injuries. The lawsuit claimed that the shoulder system failed at a higher rate than other devices on the market and caused patients to experience pain, instability, and decreased mobility. Exactech has also faced legal action related to its hip replacement products. In 2017, the company settled a lawsuit with the U.S. Department of Justice (DOJ) for $3 million. The DOJ alleged that Exactech had violated the False Claims Act by paying kickbacks to surgeons to use its hip and knee replacement products. The settlement resolved allegations that Exactech had paid kickbacks in the form of consulting fees, travel, and entertainment expenses to surgeons to encourage them to use its products. In conclusion, the Exactech knee, ankle, and hip replacement lawsuits highlight the importance of patient safety and transparency in the medical device industry. Patients who have received joint replacement implants should be aware of the risks and benefits of the devices and should consult with their healthcare providers if they experience any complications or side effects. Manufacturers have a responsibility to design and market safe and effective products and to provide accurate and complete information to patients and healthcare providers.
By Medical Claim Center1 MINUTE SURVEY FORM
https://survey.medicalclaimcenter.com/project/3
3 MINUTE SURVEY FORM
https://survey.medicalclaimcenter.com/
One of the most significant lawsuits against Exactech was filed in 2018 by a group of patients who had received Exactech Optetrak knee implants. The plaintiffs claimed that the knee implants were defectively designed and caused them to suffer severe injuries, including pain, instability, and the need for revision surgery. The lawsuit alleged that Exactech knew about the defects in its knee implants but failed to warn patients or the medical community about the risks associated with the devices. The case was consolidated into a multidistrict litigation (MDL) in the United States District Court for the Northern District of Indiana. In 2020, the court approved a $30 million settlement agreement between Exactech and the plaintiffs. The settlement resolved approximately 1,900 claims and provided compensation to patients who had undergone revision surgery or had their knee implants removed due to complications. The settlement also established a program to provide additional medical monitoring and care to patients who had received the Optetrak knee implants. In addition to the knee implant lawsuit, Exactech has faced legal action related to its ankle and hip replacement products. In 2020, a group of patients filed a class-action lawsuit against Exactech and its distributor, alleging that the Exactech Equinoxe Reverse Shoulder System was defectively designed and caused them to suffer severe injuries. The lawsuit claimed that the shoulder system failed at a higher rate than other devices on the market and caused patients to experience pain, instability, and decreased mobility. Exactech has also faced legal action related to its hip replacement products. In 2017, the company settled a lawsuit with the U.S. Department of Justice (DOJ) for $3 million. The DOJ alleged that Exactech had violated the False Claims Act by paying kickbacks to surgeons to use its hip and knee replacement products. The settlement resolved allegations that Exactech had paid kickbacks in the form of consulting fees, travel, and entertainment expenses to surgeons to encourage them to use its products. In conclusion, the Exactech knee, ankle, and hip replacement lawsuits highlight the importance of patient safety and transparency in the medical device industry. Patients who have received joint replacement implants should be aware of the risks and benefits of the devices and should consult with their healthcare providers if they experience any complications or side effects. Manufacturers have a responsibility to design and market safe and effective products and to provide accurate and complete information to patients and healthcare providers.