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Medtronic Heart Lead Recall
News Article Excerpt

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October 16, 2007
Associated Press, "Medtronic Sued Over Recalled Device"
A man who claims he received 47 unneeded jolts from his implanted defibrillator is suing Medtronic over the broken wires the company is recalling. Plaintiffs Leonard Stavish and Kelly Luisi seek class-action status in U.S. District Court in Minneapolis as representatives of people they say were hurt. The lawsuit's allegations include emotional distress and negligence, and it seeks restitution, disgorgement of profits, and punitive damages.

Medtronic Inc., maker of pacemakers and other heart devices, has acknowledged that wires connecting its implantable defibrillators to patient hearts break more often than it expected. It said five deaths may be linked to the broken wires. Medtronic said some 235,000 people have the Sprint Fidelis lead wires. Medtronic spokesman Rob Clark did not immediately return a phone message seeking comment.

Lieff Cabraser is serving a co-counsel in this litigation. Learn more about the Medtronic recall.
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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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