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Medtronic Heart Lead Recall
News Article Excerpt

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February 22, 2009
New York Times, "Medical Device Ruling Redraws Lines on Lawsuits"
The Supreme Court's decision Wednesday protecting many types of medical device makers from personal injury lawsuits began rippling through the courts and law offices almost immediately. Hours after the decision in the case, Riegel v. Medtronic, was announced, lawyers involved in a group of Florida state court cases related to Johnson & Johnson’s drug-coated Cypher heart stent received an e-mail message from Judge Mary Barzee Flores asking for briefs on whether the lawsuits should be allowed to continue.

And lawyers for patients with injuries they attribute to other devices like heart valves, artificial hips and defibrillators said they were girding for a flood of court filings from device makers like Medtronic asking judges to dismiss such lawsuits. Last fall, Medtronic recalled a product, known as the Sprint Fidelis, after reports that the leads -- wires that connected the device to the heart -- were more prone to developing potentially deadly fractures than an older lead called the Quattro.
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About Lieff Cabraser

Founded in 1972, Lieff Cabraser Heimann & Bernstein, LLP is an over sixty attorney law firm with offices in San Francisco, New York and Nashville. We represent clients in defective medical device personal injury lawsuits and other cases.

Copyright © 2012 Lieff Cabraser Heimann & Bernstein, LLP        

TRADEMARK NOTICE: "Sprint Fidelis" is a trademark of Medtronic, Inc. Lieff Cabraser is in no way affiliated with Medtronic, Inc. The use of this mark is solely for informational and product identification purposes.

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