DeGaris Law is currently investigating claims involving Exactech knee polyethylene liners which led to the need for revision surgery. A faulty oxygen seal in its packaging may have caused oxidation of the medical device’s polyethylene insert.
As shown in this diagram, a standard knee replacement has four parts:
As a result of increasing consumer complaints, the components underwent investigation. What was found, was one of the packaging layers for the plastic joint inserts may leak oxygen into the insert. This causes oxygen to diffuse into the plastic tibial insert prior to it being implanted in a patient’s knee. When a large amount of oxygen diffuses into the plastic insert before it is implanted, it leads to oxidation, which causes the plastic to wear out. A Birmingham injury lawyer may be able to work towards financial compensation for your injuries.
In August 2021, Exactech began selectively recalling devices that were in hospitals’ inventory for use in upcoming knee and ankle replacements. In 2022, a major recall was announced of all knee and ankle arthroplasty polyethylene inserts. The recalled inserts were manufactured between 2004-2022 and have been used in approximately 150,000 knee and ankle replacement surgeries. The insert systems that are covered by the recall include:
If you or a loved one had to undergo revision surgery as a result of a recalled Exactech Knee or Ankle implant, contact DeGaris Law today for a free consultation.