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d’Oliveira & Associates Issues Webpage With Current Information On Stryker Hip Implant Lawsuits
Date:1/17/2013

(PRWEB) January 17, 2013

The Food and Drug Administration (FDA) approved Stryker’s first hip implant device for sale on the market in 2003 and approved Styrker’s Rejuvenate Modular and ABG II models in 2008 and 2009 respectively. The Styker hip implant is a medical device where a metal ball connects to a metal socket to simulate the hip joint. Allegedly the metal on metal joint is corrosive and creates health problems for the patient. Serious side effects of the Stryker hip implant allegedly include pain, infection, tissue damage, bone damage, difficulty walking, broken implants, and death. The main cause of these side effects is the corrosion of metal in the body causing the device to fail and resulting in blood toxicity. The alleged failure of the Stryker hip implant has forced patients to undergo corrective surgery. The FDA has issued numerous warnings to Stryker about its packaging, cleanliness, and unsatisfactory manufacturing of its medical devices. In July 2012, Stryker issued a voluntary recall of its hip implant products, Rejuvenate Modular and ABG II. The recall warned of the two products likelihood to fail.

Stryker Lawsuits

Recently, a New York judge denied Stryker’s motion to dismiss based on the statute of limitations. Stryker claimed that the three-year statute of limitations began to run in 2007 when the plaintiff first complained of hip pain. The judge ruled that the jury could find the statute of limitations began to run in 2009 when the plaintiff’s pain escalated. This case illustrates the importance of filing a legal claim in a ti
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