If you are having complications with your DePuy Hip Replacement or Stryker Hip Replacement contact the DePuy Hip Replacement Helpline , Stryker Hip Replacement HelplineMichigan and speak to a medical social worker about you DePuy or Stryker recall. DePuy Hip Replacement Helpline lawyers and Stryker Hip Replacement lawyers are available to explain the Stryker and DePuy Hip Replacement lawsuit. Depuy Hip Recall lawyers, Stryker Hip Replacement recall lawyers accepting cases in Ann Arbor, Battle creek, Detroit, Flint, Grand rapids, Holland, Jackson, Kalamazoo, Lansing, Monroe, Muskegon, North Michigsn, PortHuron, Saginow, Upper Peninsula, and all of michigan. Call come in daily with stories of the failed dePuy, Revision surgeries and pain and suffering. We hear from parents of disabled children, adults and seniors. All whos quality of life has been changed by these hip recalls.
On August 24, 2010, DePuy Orthopedics, a subsidiary of Johnson & Johnson, announced 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 sever
e 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.
- Thigh pain
- 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
- Groin pain
- change in positioning of the hip replacement device
- Pain with weight bearing
- Loose hip cups
- Hip dislocations
- Bone fractures
- Pseudotumors from metal debris
- Allergic reactions
- 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 lawyers are accepting clients and reviewing files for all recalled hip implant victims.
- Severe limitations in daily activities and decline of quality of life
- High metal ions levels in their bloodstreams
- Loosening, when the implant does not stay attached to the bone in the right position
Cobalt and Chromium Toxicity Alert
Metallosis is a condition that can occur when the metal-on-metal movement of the implant causes friction and releases higher, potentially dangerous levels of chromium and cobalt ions into the body.
Metallosis is usually defined as aseptic fibrosis, local necrosis, or loosening of a device secondary to metallic corrosion and release of wear debris
If you have a DePuy Hip replacement you must check your blood levels for high levels of Chromium and Cobalt. A high level of toxicity is characterized by symptoms of vision impairment, hearing loss, pain, swelling, and “brain fog.” This toxicity can cause allergic reactions and even death. The complications associated with toxicity are quite serious.
What Should you Do if you have a failed DePuy Hip Replacement ?
If you have a DePuy ASR hip replacement or hip resurfacing, and are experiencing problems with the device, call the DePuy Hip Replacement Helpline and speak to a DePuy Recall attorney immediately. You should retain an attorney before undergoing a revision surgery so that potentially important evidence can be preserved. There is a limited period of time in which you may bring a legal action against DePuy or any Hip replacement manufacturer for a failed hip system, so don’t delay. Contact the DePuy Hip Replacement Helpline today.
You Must Do the following:
- If you are having complications see your Orthopedic surgeon immediately. Your health is first priority,
- If you are not having complications and you have a Metal on Metal DePuy Hip Replacement get tested for chromium and cobalt levels in the bloodstream on a regular basis
- Call the DePuy Hip Replacement Helpline for a lawyer. You must protect your rights, potential costly medical bills, pain and suffering and loss of quality of life.
DePuy Hip Replacement Helpline lawyers
If you or a loved one is suffering do to a failed DePuy and needs additional revision surgeries contact the DePuy Hip Replacement Helpline lawyers for a case review for:
- Compensatory damages
- Medical Bills
- Pain and suffering
- Loss of consortium
- Loss of quality of life
- Punitive damages
Call the dePuy Hip Replacement Helpline today.
The DePuy Hip Replacement Helpline and The DePuy lawyers 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. What has happened to people as a result of these defective hip repalcements is very sad.Not only do they have to experience this hip replacement pain, they will now have to go through radiographic evaluation, blood testing, an MRI and will probably require yet another hip revision surgery to take away and exchange the Depuy ASR Hip Implant, followed by physical rehabilitation. These batteries of tests are general for people who need to have Hip Revision Surgery with a defective hip replacement from Depuy. These effect our senior population the most who have a slow recuperation and are hoping to spend some active years enjoying life.
Bipartisan Senate bill Before Congress would go one step further then the FDA’s 510(k) approval system
Three U.S. senators recently introduced a bill to Congress that would make medical device manufacturers do more to prove their devices are safe for patients than is currently required under the Food and Drug Administration’s fast-track approval process. The bill was written with defective devices such as DePuy Orthopaedic’s metal-on-metal hip implant in mind.
Call The DePuy Hip Recall Helpline today
Stryker Hip Replacement Helpline
Michingan Stryker Hip Replacement Helpline has been launched to assist people with a failed Stryker Rejuvinate and APG II Modular stems failed component.
Stryker Hip Replacement News
A recent trial in which a Stryker hip lawyer alleged that the patents from which Stryker products were created in the 1990s was infringed upon by another orthopaedic manufacturer, Zimmer Inc., was concluded on February 5, 2013. Trial in Michigan.