Stryker ABG II hip replacements in Kentucky

Stryker ABG II hip replacements in Kentucky

Recalled Stryker ABG II hip replacements in Kentucky are problematic and anyone with one of these hips should call a Stryker ABG II hip replacement attorney today. Whether you’re young or old, sometimes joint replacements are necessary. Hip replacements are one way to preserve a certain quality of life if you’ve suffered joint damage due to age, disease or injury. However, these replacements often come with side effects. The Stryker hip replacement developed by the Michigan based company, The Stryker Corporation, was developed with multiple stem and neck parts for greater patient customization. Stryker ABG II hip replacements developed by Stryker were FDA approved without clinical testing because they were based on models that were approved in the past.

Unfortunately, even though Stryker used a titanium alloy to reduce fretting and corrosion, its subsequent use proved that metal flaking still occurred in patients, causing serious side effects. Multiple Stryker ABG II hip replacements in Kentucky arose after patients had to undergo surgeries to correct the replacement with a ceramic/metal replacement. This type of revision is problematic because of the placement of the original hip replacement’s position deep into the femur. Removing the Stryker implant can cause the femur to break during the procedure.

Stryker ABG II hip replacements in Kentucky | Lawsuits and Subsequent Recall

In July 2012, The Stryker Corporation recalled the parts that make up the Rejuvenuate and ABGII hip replacements and stopped all US and International sale and production. However, the implants were in use from 2009 to 2012, three years before the recall. Patients were urged to undergo blood tests and medical tests if they were experiencing pain and symptoms as a result of their Stryker hip replacement. As a result of the implant, some patients experienced numerous fractures as a result of bone and tissue damage caused by corrosion and fretting. Multiple Striker hip replacement lawsuits developed with the Stryker Corporation being accused of negligence because of a lack of clinical testing and inadequate warnings about possible corrosion and fretting. Stryker admitted that their devices were likely to cause corrosion and fretting near the neck junction. And, in August of 2012, the first liability lawsuit was brought against the Stryker corporation. Even though 20,000 of the devices were implanted, over 50,000 implants were sold before Stryker made their recall. This could lead to even more lawsuits once more people come forward.

Major Health Risks and Symptoms Surrounding Stryker ABG II Hip Replacements in Kentucky

Patients who have undergone a Stryker hip replacement are at risk for several painful health risks and symptoms. Because the Stryker hip replacements still has metal in them, corrosion and fretting are possible. This leads to several issues, including necrosis, metallosis, osteolysis and pain. Once metal enters the blood stream and the tissues in the body, it can cause the tissues to die. Premature death of tissues results in necrosis. This in turn can lead to bone fractures. Major surgeries are required to reverse the adverse effects of the Stryker hip replacement and they are costly, both financially and emotionally for patients. It is important that if you or a loved one has experienced pain, swelling or other symptoms related to your Stryker hip replacement, that you contact an attorney immediately. Attorney Group for Kentucky can provide you with legal counsel and help you to get redress for your Stryker ABG II hip replacements related trauma.

Major Stryker Hip Replacement Lawsuits

Stryker ABG II hip replacements in KentuckyBecause close to 20,000 Stryker implants were administered before their recall in 2012, numerous lawsuits have been filed against the Stryker Corporation. Many of these lawsuits accuse the Stryker Corporation with negligence because they failed to conduct adequate testing before releasing their product for public use and they failed to provide proper warnings about the possible side effects caused by their devices. Because they modeled their hip replacements on previous models that were known to have corrosion and fretting issues, the Stryker Corporation knew or should have known that similar issues would arise with their devices. Corporations like Stryker are held to a higher standard because they are professional medical manufacturers who are responsible for properly warning consumers of the risks of the products they manufacture.

If you have suffered as a result of a Stryker ABG II hip replacements in Kentucky, there is help for you. Contact a Attorney Group for Kentucky lawyer to help you get the help you need. An attorney can help you file your case and get the redress necessary to pay for rising medical costs associated with revision surgery and medications caused as a result of the Stryker hip replacement. You are not alone, but call our office now before it’s too late.

Thousands of people have been effected by the faulty Stryker ABG II hip replacements in Kentucky and many haven’t received compensation for their injuries. Don’t be one of them. Help is available, but it is important that you start now. Give our offices a call and our knowledgeable attorneys and staff will be able to gather information about your specific situation as well as give you the information you need to start your case.