Nebraska Hip recall lawyers and the DePuy Hip replacement Helpline are ready to help you.
If you are having complications with your DePuy Hip Replacement call the DePuy Hip Replacement Helpline Nebraska and speak to medical social worker about you recalled DePuy Hip . Hip Replacement recall Helpline lawyers are available to explain the DePuy Hip Replacement lawsuit. Hip replacement recall lawyers are ready to help you in Grand Island, Lincoln, North Platte, Omaha, Scottsbluff and all of Nebraska.
The Hip recall
On August 24, 2010, DePuy Orthopedics, a subsidiary of Johnson & Johnson, issued a global recall of the ASR™ XL Acetabular System. This total hip replacement has been available in the U.S. since July 2003. Included in the recall was the DePuy ASR™ Hip Resurfacing System, a partial replacement, only approved for use outside the U.S. The recall was initiated following a study which showed that many patients receiving the hip implants suffered from severe pain, stiffness and swelling, followed by popping and grinding sensations, which interfered with their ability to walk, stand, or sit for long periods of time. These symptoms worsened over time resulting in severe disability often requiring a second hip replacement surgery, called revision surgery.
What Is The DePuy Hip Implant Replacement ?
The DePuy ASR (Articular Surface Replacement ) hip system is a metal on metal hip replacement. In a hip replacement surgeons replace or resurface the cup, known as the acetabulum. At the same time, they replace the femoral head or the ball of the femur in the hip with the femoral ball, almost always connected to a stem that fits down in the femur. It’s a bit of a euphemism because you’re not replacing everything in the hip. It is called a total hip arthroplasty.
DePuy Hip Replacement Recall
93,000 Hip Implants have been recalled due to implant failures. These Implants have resulted in complications injuries and the need for revision surgeries.
The recall affects the ASR XL Acetabular System, which is used for total hip replacements, and the ASR Hip Resurfacing System, which is used in a newer kind of bone-conserving procedure. The DePuy hip recall was issued because data it received showed that five years after the hip was implanted, 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. This is a high and unusual amount of revisions and certainly higher then would be anticipated.
The DePuy Story
Pain upon walking
Pain when standing from a seated position
Unexplained hip pain
Metal products of the device coming off and showing in blood tests
change in positioning of the hip replacement device
Pain with weight bearing
Loose hip cups
Pseudotumors from metal debris
Permanent muscle and tissue damage
There are further concerns regarding toxicity and high levels of chromium and cobalt in the bloodstream from the rubbing of the metal components.
Additional Complications Include:
- Cement extrusion
- Immediate dislocation
Complications that can occur years after surgery can include:
- aseptic loosening
- aggressive granulomatosis,
- stress shielding
- heterotopic ossification
- and prosthetic fracture
The DePuy Hip Replacement Helpline and The DePuy lawyers Nebraska are concened about victims of the faulty DePuy. DePuy Orthopaedics recalled its ASR replacement hip system because its components can come loose, fracturing the bone around the implant, depositing metal fragments in the bloodstream, and causing pseudotumors, pain and the need for revision surgeries. The DePuy hip Replacement Helpline is hopeful that new legislation will protect victims in the future. if you have a Depuy Hip Replacement you must:
- Check your blood for toxicity and high levels of Chromium and Cobalt.
- If you are having Complications see your Orthopedic Surgeon Immediately
- Consider Revision surgery
- Contact the DePuy hip Replacement Helpline to speak to a Hip recall lawyer immediately before any revision surgery
Congress Has finally Gotten Involved
Bipartisan legislation was introduced in the US Senate that would force medical device manufacturers to track the performance of implants after they were approved for sale.
The bill would allow the Food and Drug Administration to compel companies to track implants, such as replacement hips, that belong to a category of products that do not require human testing for approval.
The Helpline lawyers are ready to help you
The DePuy Hip Replacement Helpline attorneys are concerned about the effects of these hip replacements. If you or a Nebraska loved one has a recalled hip replacement and has been told you need revision surgery, metallosos, or any other complications call the Depuy Hip replacement Helpline today,
DePuy Hip Recall lawyers are ready to help you in: Grand Island, Lincoln, North Platte, Omaha, Scottsbluff and all of Nebraska.