05/16/2022 | News release | Distributed by Public on 05/16/2022 12:41
In August 2021, Exactech® - a Florida-based medical-device manufacturer - recalled certain models of ankle, hip and knee replacement devices due to a range of potentially dangerous health issues relating to the devices failing or breaking down prematurely.
In short, the U.S. Food and Drug Administration (FDA) identified several models of Exactech ankle, hip and knee replacements made with polyethylene inserts that were packaged in a way that exposed the inserts to too much oxygen. Due to the abundance of oxygen, the inserts broke down or failed prematurely while inside patients' bodies.
Problems like these can lead to serious health complications, including the need for costly revision surgery to repair, remove or replace the defective device.
More than 7 million Americans are living with ankle, hip and knee replacements, according to the American Joint Replacement Registry (AJRR). Given how common ankle, hip and knee procedures are, potentially thousands of Americans have suffered health complications as a result of a defective Exactech device.
Exactech did not directly warn patients who have had one of their defective devices implanted. As a result, many patients are only now learning about potential implant defects after experiencing adverse symptoms and health complications.
When an Exactech implant breaks down, it can cause the device to loosen or fail, leading to potentially severe physical symptoms and mental anguish.
Physical health issues from defective Exactech ankle, hip and knee replacement products may include:
Injuries and/or conditions like those above can be painful, debilitating and life-altering. As a result, individuals experiencing the symptoms of a defective implant device may find managing everyday tasks difficult - or even impossible. In many cases, in order to address painful symptoms, revision surgery is required.
Unfortunately, revision surgery is an invasive and complex procedure that:
A recalled Exactech joint-replacement device can become a costly and life-altering burden to patients who have had such a device implanted in their bodies. The FDA's recall includes all knee and ankle inserts packaged in defective bags "regardless of [its] label or shelf life."
To see a full list of Exactech product models included in the recall, visit our Exactech recall page.
If you or a loved one has an Exactech ankle, hip or knee replacement device and is experiencing adverse side effects, it's important to speak with your doctor right away. Your doctor will be able to diagnose any complications and advise you on whether replacement surgery may be required.
You may be eligible to file an Exactech lawsuit if you:
The defective device attorneys at Simmons Hanly Conroy have a great track record in recovering compensation for individuals injured by implant devices. Recently, firm attorneys represented six individuals injured by DePuy Pinnacle metal-on-metal hip implant devices, securing a $1 billion verdict on their behalf.
For years, our firm has successfully held companies accountable for the injuries they've caused our clients, securing more than $9 billion nationwide. Contact us today to see if we may be able to help in your situation.