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Have You Been Affected By the Stryker Hip Recall?
Of course it is hoped that you will never need to consult a Texas Stryker hip lawyer, however if you are a recipient of the recalled Stryker ABGII or Rejuvenate hip implant, you could very well benefit from knowledgeable legal representation. The Rejuvenate received FDA approval in 2008, and the ABGII in 2009. The strong marketing push began in February, 2010, yet less than three years later, the FDA began receiving adverse event reports regarding injuries and negative health symptoms associated with the two devices. A field safety notification was sent out to physicians and hospitals in April, 2012, describing the potential hazards associated with the two hip devices, including a higher-than-normal rate of failure. In fact, the Australian Registry placed the failure rate of the two devices at 8.1%--considerably higher than for most other hip implants.
Subsequent research has placed the failure rate of the ABGII and Rejuvenate devices anywhere between 8% and 65%. Since approximately 20,000 of the devices were sold prior to the Stryker hip recall, there is a very good chance that even recipients of the recalled devices who have not yet experienced difficulties may well do so in the future. Following the Stryker hip recall in July, 2012, those injured by the defective devices began filing suit against Stryker. To date, there are over 1,700 lawsuits pending against Stryker, and as the statutes of limitations grow near for those in some states, it is expected that many more will follow. If you are a victim of the Stryker hip recall, it is important that you speak to an experienced Texas Stryker hip lawyer regarding your injuries, the Texas Stryker hip statute of limitations and the possibility of joining others harmed by a defective Stryker device in a Texas Stryker hip lawsuit.
What are the Problems Associated with the Stryker Rejuvenate and ABGII?
You may have experienced problems with metallosis (pain in the hip, groin or thigh, degradation of the bone and tissue surrounding the implant, acute inflammation and total hip failure). If so, you will likely be required to undergo revision surgery—or have already done so. Stryker revision surgery is more expensive as well as riskier than the original hip implant surgery and could leave you with a long recovery time as well as a pile of medical bills. Symptoms of metal toxicity can occur when cobalt and chromium ions reach the bloodstream, after shearing away from a corroded metal hip implant. Metal toxicity can cause serious medical issues such as: kidney disorders, neurological and cardiovascular disorders, loss of hearing and vision, headaches, irritability, anxiety, depression, vertigo, skin rashes, memory loss, thyroid and gastrointestinal disorders, reproductive disorders and the development of pseudo-tumors.
The Effects of the Texas Stryker Hip Statute of Limitations
The Texas Stryker hip statute of limitations governs the amount of time you have in which to file a lawsuit against the manufacturer of a defective product or device.
While the statutes differ from state to state, in the state of Texas any civil cause of action for a product liability case must be filed within two years of the time the injury occurs.
It is crucial that you speak to an experienced Texas Stryker hip lawyer in order to determine when your specific statutes will run. You may be eligible to file a Texas Stryker hip lawsuit which can pay medical expenses associated with the Stryker hip recall as well as compensate you for pain and suffering.
Because the Texas Stryker hip statute of limitations can be extremely complex, there is no way for you to really know when the statutes will expire in your case without benefit of meeting with a Texas Stryker hip lawyer.