!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 theStryker Master Settlement Agreement here.
Have You Been Affected by the Stryker Hip Recall?
The Stryker Rejuvenate and ABGII received FDA approval in 2008 and 2009; Stryker began marketing the two metal hip implants in earnest in early 2010. At the time the implants were released, Stryker claimed that, due to the groundbreaking design, the Rejuvenate and ABGII would last much longer than traditional implants and would be much safer than other metal-on-metal implants due to the use of a ceramic ball. Stryker offered a variety of components in different lengths and angles which allowed surgeons to custom-fit the device to the individual patient, however even this innovation did not outweigh the risks. The FDA began receiving adverse event reports within the first year—by early 2012, over 300 adverse reports had come in to the agency.
At the time of the recall, Stryker stated the Rejuvenate and ABGII had a higher-than-normal rate of failure, and were likely to experience fretting and corrosion at the neck junction, during periods of patient activity. This fretting and corrosion would then lead to excess cobalt and chromium ion debris shearing away from the implant and landing in the hip tissues or traveling to the bloodstream. If you have suffered serious injury following the Stryker hip recall, it is important that you contact an experienced Florida Stryker hip lawyer as soon as possible. Your Florida Stryker hip lawyer can ensure your rights are protected and can handle all the details concerning your Florida Stryker hip lawsuit.
Metallosis and Metal Toxicity Associated With the Stryker Hip Recall
Perhaps you are already aware of injuries you’ve suffered which are directly related to the Stryker hip recall, or perhaps you have not yet experienced any adverse health issues related to your Rejuvenate or ABGII. Either way, you must speak with a skilled Florida Stryker hip lawyer; even those who currently have no symptoms have a significant risk of developing problems associated with the Stryker hip recall in the near future. Metallosis can occur when the cobalt and chromium ions lodge into hip tissues, causing chronic pain, severe inflammation, loss of tissue and bone, total hip failure and the necessity for hip revision surgery. When those ions end up in the bloodstream, the following issues can result:
· The development of pseudo-tumors
· Irritability, anxiety, depression
· Memory loss
· Disruption of DNA
· Loss of hearing and vision
· Gastrointestinal disorders
· Neurological and cardiovascular disorders
· Renal and thyroid issues
· Reproductive disorders
How the Florida Stryker Hip Statute of Limitations May Affect You
One of the most important considerations may be the Florida Stryker hip statute of limitations. While the statutes of limitations differ from state to state, in Florida, any civil cause of action for a product liability case is governed by the 2011 Florida Statutes, Title VIII, Chapter 95, Section 11,(3)(o), which indicates that these types of cases must be filed within four years of the time the injury is discovered or should have been discovered.
While the Florida statutes are longer than many other states, it is nonetheless extremely important that you discuss your potential Florida Stryker hip lawsuit with a highly skilled Florida Stryker hip lawyer in order to know for sure when the statutes began running in your case. The Florida Stryker hip statute of limitations can be complex, therefore allowing an experienced attorney to review your case is your very best course of action. A well-qulaified Florida Stryker hip lawyer will work hard on your behalf in pursuing compensation for your injuries related to the Stryker hip recall.