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Harm Caused by the Stryker Hip Recall:
Over 1,700 lawsuits have been filed against Stryker Corporation, the manufacturer of the recalled Rejuvenate and ABGII. One of those, filed by a man in California, alleges Stryker failed to disclose the high rate of failure of the Rejuvenate and neglected to inform the FDA of serious side effects, even after being made aware of the potential defects of the two devices. This lawsuit—like many others against Stryker—asserts that, due to design and manufacturing defects, the devices were not constructed to ensure there would be no excessive corrosion or deterioration.
Such metal ion debris can travel to the bloodstream or lodge in the patient’s hip tissues, creating serious health issues. Metal ions which burrow into the tissues surrounding the hip can result in the patient having to undergo hip revision surgery. These ions can also cause serious levels of inflammation, pain, degradation and death of surrounding bone and tissue and total hip failure. When the tiny metal shards enter the bloodstream, the following health issues can result:
· Gastrointestinal disorders
· Loss of hearing and vision
· Memory loss
· Depression, anxiety, irritability
· Reproductive disorders
· Neurological and cardiovascular disorders
· Renal and thyroid disorders
· The development of pseudo-tumors
· Skin rashes
What You Must Know About the Indiana Stryker Hip Statute of Limitations
Individual states have statutes of limitations which range from one year all the way to six years, with most of the states having a two-year statute. Indiana is one of those with a two year statute of limitations, which begins to run on the date of the injury. Indiana also has a ten-year statute of repose—the statute of repose is triggered by an event, rather than an injury, such as the date the device was manufactured or sold.
If you are a resident of Indiana and have been harmed by the Stryker hip recall, it is important that you have a solid understanding of the statute of limitations restrictions placed on your potential Indiana Stryker hip lawsuit. Only an experienced Indiana Stryker hip lawyer can accurately assess your specific case and determine when your Indiana Stryker hip statute of limitations will expire.
FDA Approval of the Stryker Rejuvenate and ABGII
The FDA approved the Rejuvenate in 2008 and the ABGII in 2009, however marketing for both devices did not begin in earnest until February, 2010. Even so, during 2010, over 60 adverse event reports were sent to the FDA regarding the ABGII and Rejuvenate. Surgeons who were forced to remove the implants from their patients noted a substance which looked like “black rust,” as well as a milky substance in the hip tissues. Patients noted symptoms of metallosis and metal poisoning.
If you have suffered harm or injury due to the Stryker hip recall, it is important to speak to a knowledgeable Indiana Stryker hip lawyer as soon as possible in order to avoid having the Indiana Stryker hip statutes of limitations run. You may have serious medical costs associated with revision surgery or other health issues related to the Stryker hip recall—if so, your attorney can help you determine whether filing an Indiana Stryker hip lawsuit is in your best interests.