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Stryker Hip Replacement Lawyers, Stryker Hip Replacement Recall News

Written by lisaspitzer on . Posted in Connecticut Multidistrict Litigation Lawyers, Delaware Multidistrict Litigation Lawyers, Florida Multidistrict Litigation Lawyers, Georgia Multidistrict Litigation Lawyers, Illinois Multidistrict Litigation Lawyers, Indiana Multidistrict Litigation Lawyers, Iowa Multidistrict Litigation Lawyers, Kansas Multidistrict Litigation Lawyers, Maine Multidistrict Litigation Lawyers, Michigan Multidistrict Litigation Lawyers, Minnesota Multidistrict Litigation Lawyers, Mississippi Multidistrict Litigation Lawyers, Nevada Multidistrict Litigation Lawyers, New Jersey Multidistrict Litigation Lawyers, New York Multidistrict Litigation Lawyers, Ohio Multidistrict Litigation Lawyers, Oklahoma Multidistrict Litigation Lawyers, Oregon Multidistrict Litigation Lawyers, Pennsylvania Multidistrict Litigation Lawyers, Product Recall News, Texas Multidistrict Litigation Lawyers, Utah Multidistrict Litigation Lawyers, Washington DC Multidistrict Litigation Lawyers, Washington Multidistrict Litigation Lawyers, West Virginia Multidistrict Litigation Lawyers, Wisconsin Multidistrict Litigation Lawyers, Wyoming Multidistrict Litigation Lawyers

The Stryker Rejuvenate Hip Recall for metal toxicity was a surprise to many patients and doctors because it is not a metal on metal hip. In fact, many patients selected this hip to avoid the metallosis problem that has been in the news for the last two years since the DePuy ASR metal on metal recall in August of 2010.

The Stryker Rejuvenate hip is made with a ceramic ball and a polyethylene liner in the acetabular cup. The recalled DePuy ASR and the recalled Smith & Nephew R3 hips both have a metal ball and a metal cup which is called a metal on metal articulation. The problem with the metal on metal hips is that the metal on metal interface generates metallic debris that is toxic to the tissues in the hip compartment causing fluid buildup, tissue damage, and failure of the implant.

A lawsuit claiming that Stryker Corporation was negligent and did not adequately warn patients about the risks associated with its Trident hip replacement system was filed in the Superior Court of the State of Indiana for the County of Marion by plaintiff Darlene A. Gray. On the 5th of September, 2012, the suit was removed under federal diversity jurisdiction. The lawsuit claims that plaintiff Gray had the Trident hip system implanted after suffering from avascular necrosis of the right hip for a number of years, however, the device failed much earlier than what would be reasonably expected, she was forced to undergo Stryker revision surgery in order to correct complications she was experiencing as a result of her implant.
Recall issued over parts

Stryker issued a recall of two component hip parts related to their Trident hip replacement system in 2008, as a number of patients came forward with assertions of pain related to their Trident hip implants. In addition, squeaking and popping sounds and sensations were reported by a number of patients, which could be embarrassing as well as indicative of other complications associated with the products. Some patients reported even more serious complications, including implant failure and bone fractures. A number of these patients had to undergo revision surgery in order to correct them.

The plaintiff is seeking compensation based on damages associated with medical expenses and pain and suffering that she has experienced as a result of her use of the allegedly defective product. She is making claims of negligence and defective product claims against Stryker Orthopedics.
Lawsuits consolidated in New Jersey

A number of patients have chosen to go ahead with Stryker hip litigation after experiencing serious complications linked to the devices, and a consolidation of a number of lawsuits has taken place. Some lawsuits have been consolidated in the New Jersey Superior Court of Atlantic County and are being presided over by Judge Carol Higbee.

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