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How the Stryker Hip Recall May Affect You:
If you are the recipient of a Stryker Rejuvenate or ABGII hip implant, then you may be aware of the Stryker hip recall which occurred in July, 2012. Over 20,000 patients received one of these recalled implants between the time of FDA approval in 2009 and the time of the recall, just three years later. At the time the Rejuvenate and ABGII hip devices were released, they were advertised as being highly innovative—as well as safer than other metal-on-metal hip implants due to the use of a ceramic ball rather than a metal ball. A variety of neck and stem components also allowed surgeons to construct a hip implant device which could be custom-fit to the individual patient, according to the patient’s activity levels, size and body type.
Unfortunately, within a year of the release of the two implants, patients and surgeons began contacting the FDA regarding issues associated with the devices. As early as July, 2010, one surgeon noted significant fretting at the neck/stem junction as well as obvious tissue degradation attached to a patient’s implant, and in 2011, another surgeon noted corrosion resembling “black rust” on a patient’s Rejuvenate implant. In 2011 alone, over 130 adverse reports involving a Stryker Rejuvenate or ABGII came into the FDA, with many patients experiencing severe pain, massive metallosis and symptoms of metal toxicity.
By early 2012, the number of adverse reports climbed to 300, with failure of the two hip implant devices in other countries on the rise as well; the Australian Registry calculated the failure rate of the ABGII to be as high as 8.1% in the first year following implantation. Other research places the failure rate of the ABGII and Rejuvenate anywhere from 12% to as high as 65%, meaning that even those who have yet to experience adverse effects from the Stryker hip recall, may well experience them in the future.
How the Arkansas Statute of Limitations May Affect You
The statutes of limitations in each state limit the amount of time consumers have to file a lawsuit for harm suffered from a defective device. The Arkansas statute of limitations allows three years from the time the injury is discovered—or should have been discovered—for a civil cause of action to be filed. It is extremely important that you speak to a knowledgeable Arkansas Stryker hip lawyer regarding your Arkansas Stryker hip statute of limitations. There are many variables associated with statutes of limitations which only a knowledgeable Arkansas Stryker hip lawyer can correctly interpret.
Why You Should Contact an Arkansas Stryker Hip Lawyer
Your Arkansas Stryker hip lawyer can fully assess your individual circumstances, determining whether an Arkansas Stryker hip lawsuit is right for you. To date, over 1,700 lawsuits have been filed against Stryker, with many more expected as the statute of limitations window of opportunity narrows for those in many states. Because the statutes of limitations can be complex, having a skilled Arkansas Stryker hip lawyer by your side can give you peace of mind. You can be confident that your attorney will not let your Arkansas Stryker hip statute of limitations pass, leaving you injured, with no legal course of action against the company responsible for your injuries. If you have been adversely affected by the Stryker hip recall, contact an experienced Arkansas Stryker hip lawyer to discuss the possibility of an Arkansas Stryker hip lawsuit.