Depuy Hip Recall Affects South Floridians
Depuy Orthopedics has announced a recall on all DePuy ASR XL Acetabular Systems and the ASR Hip Resurfacing Systems used in hip replacement surgeries after 2003. Early estimates show that the defective Depuy products were used in approximately 93,000 hip replacmenet surgeries worldwide. If you had a hip replacement surgery after 2003, it is important that you check your records and contact your doctor immediately to determine if you are affected by this recall.
Complaints and complications associated with Depuy artifical joint include loose hip cups,dislocations and additional fractures or muscle damage. Some people have reported increased movement of the joint, popping or clicking sensations and a decreased range of motion in the hip. The defective product has also been shown to cause metallosis, a condition caused by movement of the implant which may result in the release of higher, potentially dangerous levels of chromium and cobalt ions into the body.
Studies have shown that 12% of patients who had received the ASR Resurfacing System and 13% of patients who received the ASR total hip replacement needed to have it replaced through a revision surgery. This is an extraordinarily high failure rate for a prosthetic device. Most hip replacement are expected to last in excess of 15 years.
Depuy Offers Payment for Revision
On its Website, Depuy Orthopedics, which is owned by Johnson & Johnson, has initiated the recall and states that DePuy intends to cover reasonable and customary costs of testing and treatment associated with the ASR recall, including revision surgery if it is necessary. However, what most people don't realize is that by agreeing to participate in Depuy's program, they will likely be giving away certain rights. Depuy mentions nothing about compensating the people injured by its defective proudct for their pain, suffering, mental anguish and other intangibles.
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