If you have recently undergone knee replacement surgery with an Exactech knee replacement, you may be eligible to file an Exactech Knee Recall Law suit. You may be entitled to receive compensation for your medical bills and lost wages, as well as punitive damages. Punitive damages are intended to punish Exactech for its negligence. If you do decide to file a recall lawsuit, however, you must keep in mind that any settlement you receive may prevent you from filing any further lawsuits.
Exactech’s defective packaging caused premature failure of the polyethylene component
A Class II recall of knee implants by Exactech was announced in February 2022. Exactech sent a letter to hospitals, health care professionals, and surgeons warning that the polyethylene components in its knee implants could deteriorate prematurely, requiring surgical removal. The defect was discovered after the manufacturer discovered that the vacuum bags used to package the knee implants were nonconforming. Oxygen exposure was a significant Defective Exactech Knee Replacement cause of premature failure of the polyethylene component.
The company is currently seeking MDL status for these lawsuits, which would consolidate all of the Exactech recalls in the Eastern District of New York. Regardless of whether it is a federal or state lawsuit, the MDL process would allow the plaintiffs to file one lawsuit based on the entire Exactech recall. In the meantime, the company will be required to pay attorneys’ fees.
Exactech’s sales reps did not report the removed component to the FDA
In an effort to avoid being fined, Exactech recalled one of its products and retracted its marketing claim. Exactech’s founder, William Petty, is a prominent figure in the biotechnology industry. Previously, he was a professor at the University of Florida’s College of Medicine, where he held various positions before becoming the company’s Chief Executive Officer in 2007. He holds an M.B.A. in accounting from the University of Miami and a B.S. in business administration from the University of Memphis.
The recalled Exactech device is not a cure-all for a defective medical device. It can cause serious injuries or even death. According to the FDA, new medical devices are not tested on humans as rigorously as drugs. This lack of testing has led to an increased number of recalls in the last decade. Therefore, it’s imperative to file a lawsuit against the company if you or a loved one has suffered an injury as a result of an Exactech device.
Exactech’s sales reps promoted the implant system without alerting surgeons or patients to the problem
The resulting defect in the Exactech knee implant system can lead to significant pain, loss of knee mobility, and the need for corrective revision surgery. Exactech recently sent a letter to doctors instructing them to stop using the implants in all knee and ankle replacement surgeries. It also instructed hospitals to return the implant inventory for replacement. While this letter may seem harsh, it is entirely reasonable. It is also the only solution that Exactech has come up with so far.
Despite the growing list of complaints, the company has refused to recall the device despite knowing it was associated with an abnormally high rate of failures. In addition to the “silent” recall, Exactech’s sales reps promoted the implant system without alerting doctors and patients to the problem. This is why a search of MAUDE only returns about 500 complaints.