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In November 2011, the FDA issued a Class 1 recall of the St. Jude Medical Riata and Riata ST Silicone Endocardial Defibrillation Leads. The FDA noted evidence that the silicone insulation covering the leads is at risk for premature abrasion and externalization. As a result of the defective leads, patients may not receive the therapy when needed and in some instances are receiving unnecessary shocks.
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"For patients, having a recalled device like the St. Jude Riata leads implanted in their bodies, can be an agonizing experience. If their particular device has failed or fractured, they may need to undergo a very dangerous and complicated surgery to either extract the leads or cap them," said Reza Torkzadeh attorney at TorkLaw who is representing clients Nationwide.
The lawsuits by TorkLaw have been filed in both State and Federal Courts in Los Angeles, California where St. Jude Medical, Inc. manufactured the Riata leads. The first trial is set for February 2015 in the U.S. District Court for the Central District of California in front of U.S. District Judge James V. Selna.
"Victims and individuals who have been effected by complications related to their heart devices are encouraged to immediately check with their physicians about any potential failures and defects in their hardware," said Torkzadeh.
There are strict deadlines in which patients can make a claim. Should you believe to have one of the devices and have suffered any injuries, TorkLaw is providing free evaluations of your case today – Call Now 888.222.8286 or visit www.torklaw.com
SOURCE The Torkzadeh Law Firm
