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The Stryker Hip Recall—and How It May Have Affected You:
Over 20,000 consumers received a Stryker ABGII or Rejuvenate hip implant device between the time the two devices were released, in February, 2010, until the recall in July, 2012. Prior to the recall, Stryker issued an Urgent Field Safety Notification to hospitals and surgeons stating the Rejuvenate and ABGII were subject to a high rate of fretting and corrosion at the neck junction, leading to the release of cobalt and chromium ions into the body. Many believe the safety notification was a public relations tactic, meant to minimize the effect of the inevitable recall, and speaking to a Kentucky Stryker hip lawyer is the best way to determine how you will be affected by the Stryker hip recall.
In the end, the design claimed to offer patients longevity as well as safety failed to deliver on those claims. The Australian Registry placed the failure rate of the recalled Stryker implants at 8.1%--an unacceptably high number when compared to the “normal” failure rates less than 3%. Later research would place the Stryker failure rate much higher—some claimed the rate was as high as 65%. The Stryker hip recall could potentially end up with more plaintiffs than the DePuy ASR recall, and while about 1,700 recipients of a recalled Stryker hip implant have currently filed suit against the company, that number is expected to continue to rise as the statutes of limitations grows close for residents of certain states.
Health Issues Associated With the Stryker Hip Recall
The symptoms of metallosis include deterioration of bone and tissue surrounding the artificial implant, pain in the groin, hip and thigh area, significant levels of inflammation and total hip failure. When hip failure or significant levels of adverse health problems occur, revision surgery may become necessary, however revision surgery can be more dangerous and painful than the original surgery bringing a longer recovery time as well. When the metal parts of the hip device rub against one another, microscopic metal ions shear away from the implant, finding their way into the bloodstream as well as the hip tissues. This can lead to serious health issues such as:
· Disorders of the gastrointestinal tract
· Serious skin rashes
· Neurological, renal, thyroid and cardiovascular disorders
· Heart attack and stroke
· Disorders of the reproductive system
· Loss of vision and hearing
· Memory loss
· Irritability, anxiety, depression
· DNA disruption
· An increase in certain types of cancers
Could You Be Affected By the Kentucky Stryker Hip Statute of Limitations?
Kentucky has one of the shortest statutes of limitations of all the states, allowing only one year from the date the injury occurs in which to file a civil cause of action for a product liability case. This statute includes the caveat that should injury, death or property damage not occur within a period of eight years from the time of the product’s first use, a presumption exists that there is no defect in the product. The Kentucky Stryker hip statute of limitations can be quite complex to decipher, therefore it is in your best interests to speak to a Kentucky Stryker hip lawyer at the earliest possible opportunity.
It is imperative that you not end up injured by a device you believed to be safe, with no recourse for recovering the extensive medical expenses you may incur. Your Kentucky Stryker hip lawyer will thoroughly assess the specific circumstances surrounding your case, then help you determine whether a Kentucky Stryker hip lawsuit is your best course of action. Don’t get left out in the cold—contact a knowledgeable Kentucky Stryker hip lawyer today to discuss how the Stryker hip recall has affected your health and your future.