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Medtronic Heart Lead Recall | Medtronic Recall FAQ
Quick Facts on the Recall | Know Your Legal Rights
Resources and Documents | Recall Attorney Contact
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Clients represented by our firm filed the first personal injury lawsuits in the nation against Medtronic.

We have been appointed to a leadership role among plaintiffs' counsel in the litigation against Medtronic in federal court.

Our injury lawyers have years of experience successfully representing clients in personal injury cases. We provide each client with high-level individualized representation.

There is no charge or obligation for our review of your injury lawsuit.

We have retained product safety and medical experts nationwide to assist our clients with their claims.

In addition to a team of experienced lawyers, we have dedicated nurses, legal assistants and case clerks to assist our attorneys in the Medtronic recall litigation. Our firm has six full-time nurses, including ones with decades of experience working with heart patients.

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Lieff Cabraser represents persons across America injured by the Medtronic Sprint Fidelis heart lead. Click here to contact an experienced injury attorney at Lieff Cabraser for a free case evaluation. Or call us toll-free at 1-800-948-2181.

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Image: Newspaper  Medtronic News

Read excerpts from the latest news covering the Medtronic recall and lawsuits:

Read excerpts from the latest news covering the Medtronic recall and lawsuits

Lieff Cabraser had been investigating patient complaints concerning the Medtronic heart lead prior to the recall announced by Medtronic. On the same day as the recall, heart patients nationwide represented by Lieff Cabraser and co-counsel filed separate personal injury and class action lawsuits against Medtronic.

May 16, 2008
"Heart Device Patients Often Unaware of Recalls"

May 7, 2008
"Medtronic to Cut About 1,100 Jobs"

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Medtronic Heart Lead Recall
News Article Excerpt

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October 15, 2007
The Associated Press, "Medtronic Recall: Medtronic sued for Faulty Lead"
Recalls had already battered the heart device industry when Medtronic warned doctors that the wires connecting a patient's heart to its implantable defibrillators break too often. Medtronic told doctors to stop using the Sprint Fidelis wires after linking five deaths to breaks in them. The company said the Fidelis wires failed slightly more often than the thicker wires they were meant to replace. The problem does not affect Medtronic pacemakers.

Dr. Robert Hauser, a whistleblower in the recall of Guidant defibrillators, applauded Medtronic's decision to halt the use of Sprint Fidelis wires as "obviously the right thing to do." "I would like to have seen them take it off the market earlier," said Hauser, a senior consulting cardiologist at the Minneapolis Heart Institute at Abbott Northwestern Hospital in Minneapolis.

Hauser and colleagues published a study in July in the medical journal HeartRhythm that concluded the leads are prone to early failure, and recommended limited use until the problem is fixed. Medtronic and the FDA had a copy of their manuscript in February, he said. The company probably didn't act earlier because there was no consensus in the medical community about the leads, he said. "This really came to a head in the past month when there was a crescendo of reports and of events that may have been more concerning, including deaths," Hauser said.
  
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About Lieff Cabraser

Founded in 1972, Lieff Cabraser Heimann & Bernstein, LLP is an over fifty attorney law firm with offices in San Francisco, New York and Nashville. For the last five years, the National Law Journal has recognized Lieff Cabraser as one of the top plaintiff law firms in America.

To learn more about the advantages our lawyers offer clients in personal injury and wrongful death cases, click here.

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TRADEMARK NOTICE: "Medtronic" 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.