Medical device manufacturer Stryker Orthopedics voluntarily recalled its ABG II modular-neck hip stem in July 2012. The company chose to do so following an increasing number of reports submitted by recipients who were allegedly experiencing early device failure. While the devices were designed to last 15 to 20 years, in some cases, patients reported that that their artificial hips were failing just two to three years after the initial implantation.
Attorney Group for New York is offering free, no-obligation consultations to those who are experiencing complications with their ABG II hip stem. If you are considering filing a New York Stryker hip replacement lawsuit to recover damages for their injuries, or if you would like o learn more about your options, contact Attorney Group for New York today.
Recipients Report Early Device Failure, Other Complications
The ABG II hip stem was approved by the U.S. Food and Drug Administration (FDA) in November 2009. The system features four separate components, including a ball, a metal neck, a femoral stem, and an acetabular cup. According to Stryker, the ABG II was designed for use in younger, more active patients because the extra components were intended to provide patients with a greater range of motion.
However, recipients who are currently pursuing claims against Stryker allege that more parts meant more problems. Metallosis, for instance, is one of the most commonly reported complications and can occur when the two metal parts rub together and cause shards of cobalt and chromium to be deposited into the patient’s bloodstream, resulting in metal poisoning.
In the company’s recall, Stryker acknowledged that these high levels of metal could potentially cause a recipient to suffer from swelling and adverse local tissue reactions. In addition, you may be entitled to file a New York Stryker hip replacement lawsuit if you also suffered from difficulty walking, temporary or permanent disability, pain, trouble maintaining balance, and early device failure.
Patients Allegedly Require Revision Procedures
According to court documents, many recipients of the ABG II hip stem required removal or revision procedures to correct the complications allegedly caused by the device. However, in some cases, these surgeries were not always successful, and several patients were unable to regain their mobility. If you or a loved one is currently facing mounting medical expenses because of the treatments, rehabilitation, and other costs associated with your injury, consider seeking legal counsel to determine whether you are eligible to file a New York Stryker hip replacement lawsuit.
Plaintiffs accuse the manufacturer of releasing a defective product and failing to adequately test the hip replacement device before making the product available to consumers. Plaintiffs also allege that Stryker failed to warn the public and medical communities of the risks and possible complications associated with the ABG II, including early device failure and metal poisoning.
Contact Us Today for More Information about Your New York Stryker Hip Replacement Lawsuit
If you or someone you love was fitted with the Stryker ABG II hip stem and experienced adverse side effects or complications, you may be eligible to file a New York Stryker hip replacement lawsuit and seek compensation for your injuries. Contact Attorney Group for New York today for more information about your legal options and to receive a free, no-obligation case evaluation. If it is determined that you are entitled to recover damages, Attorney Group for New York can connect you with an affiliated ABG II lawyer who can assist you throughout the legal process. Call today.
