!STRYKER HIP SETTLEMENT ALERT! Stryker Hip Implant Recipients TAKE NOTE - Stryker Corporation has reached a 1.4 billion dollar settlement in its metal hip implant MDL. Learn all about the Stryker Master Settlement Agreement here.
Understanding the Missouri Stryker Hip Statute of Limitations The statutes of limitations can be extremely important to those harmed by the Stryker hip recall.
. The state of Missouri has one of the longer statutes as it operates under a five-year statute of limitations for product liability cases, which begins on the date injury occurs.
If you are a Missouri resident who has suffered injury from a recalled Stryker Rejuvenate or ABGII hip implant, it is extremely important that you not become complacent, thinking you have plenty of time in which to file a Missouri Stryker hip lawsuit. There are many variables associated with the Missouri Stryker hip statute of limitations, making it imperative that you speak to a knowledgeable Missouri Stryker hip lawyer.
In fact, only a qualified Stryker hip attorney can assess the circumstances surrounding your injuries and determine just when the Missouri Stryker hip statute of limitations will run in your case.
What Went Wrong With the Stryker Rejuvenate and ABGII? At the time of their release in February, 2010 (after receiving FDA approval in 2008 and 2009), both Stryker models were highly touted as being not only safer than other metal-on-metal hip implant devices, but as being much more long-lasting, as well. In fact, Stryker claimed the Rejuvenate and ABGII could last from 15-20 years, making them perfect for use in younger, more active patients requiring hip implants. Due to the use of a ceramic (rather than metal) ball, Stryker also claimed there would be much less chance of fretting and corrosion, leading to the release of excess cobalt and chromium ions into the body.
These claims largely turned out to be less than true. Within the first year after implantation, many patients were forced to have their Stryker hip device removed due to serious health issues resulting from the implant. Surgeons and patients alike sent adverse event reports to the FDA, with an accumulation of over 300 of the reports by the time of the recall. Many of the more than 1,700 plaintiffs who currently have a Missouri Stryker hip lawsuit filed against the company have alleged Stryker was well aware of the issues associated with the Rejuvenate and ABGII long before the recall was issued, potentially putting many more patients at risk.
Why File a Missouri Stryker Hip Lawsuit?
As a consumer who may be affected by the Stryker hip recall, you may wonder whether you should hire a Missouri Stryker hip lawyer, particularly if you have not yet suffered any particular ill effects. The Australian Registry placed the failure rate of the Rejuvenate and ABGII at 8.1%and further research has placed the number anywhere from 11-65%. This means that a significant number of those with a recalled Stryker hip implant may suffer some level of injury or harm.
You may have symptoms of metallosis (acute pain, inflammation, destruction of tissue and bone or total hip failure), or symptoms of cobalt and chromium poisoning (renal, thyroid, cardiovascular, neurological and gastrointestinal disorders, irritability, depression, anxiety, reproductive disorders, vertigo, memory loss, the development of pseudo-tumors, skin rashes, vision and hearing loss and the development of certain types of cancers). You could potentially end up with compromised health, financial problems and a compromised future as the result of the Stryker hip recall. Don’t wait—contact a knowledgeable Missouri Stryker hip lawyer today.