If you or a loved one has been injured as a result of a defective Cypher Stent, you may be entitled to compensation.

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We have compiled the latest news on the Cypher Stent. All of the news articles on this page require Adobe Acrobat to view.

If you or a loved one has been injured by a Cypher Stent and you would like more information about your legal rights, please contact us.

A dispute over the safety of heart stents from Johnson & Johnson and Boston Scientific Corp. is causing a public rift among cardiologists.

Doctors at a scientific conference in Washington this week are at odds over new data showing the companies' best-selling stents may cause more life-threatening blood clots than initially anticipated. The stents, which generated more than $5 billion in 2005 sales, are metal tubes that keep coronary arteries open to prevent heart attacks.

With drug-eluting coronary stents implanted in more than 2 million people worldwide, some doctors and researchers are now concerned about a long-term problem they see in a small number of patients who have received stents: blood clots inside the stents themselves.

Although the rate of serious clotting is extremely low, with manufacturers reporting just a handful of clots in more than 1,500 patients they are following, the cases concern doctors because clots nearly always cause heart attacks or death.

Doctors report an increase in potentially deadly blood clots in patients' arteries that have been implanted with drug-coated stents.

Signs of increased clotting could reduce cardiologists' and patients' enthusiasm for drug-coated stents, which are by far the most popular kind. Since hitting the market in 2003, drug-coated stents have been implanted in three million people worldwide.

The Food and Drug Administration (FDA) today updated and clarified information for physicians about adverse events associated with Cordis Corporation’s Cypher Coronary Stent. FDA posted the new information on its web site as a public health notification to physicians.

In October, FDA notified physicians about reports of thrombosis (clotting) occurring within 30 days after the device was implanted and about reports of possible hypersensitivity reactions. The agency asked doctors and patients to report any such incidents to the FDA.

O'Steen & Harrison, PLC presently is investigating legal claims on behalf of those injured by defective Cypher stents.

If you or a loved one has been injured by a Cypher stent and you would like more news about the Cypher lawsuit, just call us toll-free at 1-800-883-8888 or complete this online contact form.