Medtronic Recall News | Medtronics Lawsuit | Medical Device Safety Act Legislation Update 2009

Since the Medtronic recall of Sprint Fidelis heart leads in October 2007, patients are continuing to suffer from the life threatening consequences of a fractured defibrillator lead with no real legal recourse. Following the 2008 Supreme Court decision Riegel v. Medtronic, patients and families have been prevented from having the right to file a viable Medtronics lawsuit to help cover medical bills, lost wages and pain and suffering based on FDA preemption. In the 2008 case, the court decided that the Food, Drug, and Cosmetic Act preempts (prevents) state-law damages lawsuits brought by patients who have been injured by medical devices (like the Medtronic Sprint Fidelis leads) that were approved by the Food and Drug Administration (FDA).

We are continuing to fight for patients who have been affected by the Medtronic recall of Sprint Fidelis leads, however this legislation is very important for patients who have already suffered from a broken lead along with patients of other medical devices.

On May 12, 2009 there was a hearing on H.R. 1346, the Medical Device Safety Act of 2009. This legislation would overturn the 2008 Riegel Supreme Court decision and allow patients injured by medical devices the right to bring a claim for compensation. This legislation would also help remove harmful medical products from the market even if they were initially approved by the FDA. This benefits all patients by helping make sure that safe medical products are in the marketplace. The Medical Device Safety Act is vitally important for victims of defective Medtronic defibrillator leads who are currently left without any meaningful legal options and patients in general who use FDA approved medical devices.

The following are links to the House of Representative testimony along with video of the hearing.

David Vladeck, J.D., Professor of Law, Georgetown University Law Center
William H. Maisel, M.D., M.P.H., Director, Medical Device Safety Institute
Gregory Curfman, M.D., Editor, New England Journal of Medicine
Bridget Robb, Gwynedd, Pennsylvania
Richard Cooper, Partner, Williams & Connolly LLP
Michael Kinsley, Seattle, Washington


  

We represent all Medtronic recall clients on a contingency basis which means that there are never any legal fees unless we win compensation in your case. For a free no-obligation consultation please call toll free at 1-888-343-5375 or fill out our short online contact form and a Medtronics lawsuit attorney will contact you to answer any of your questions.

We are continuing to fight for patients rights who have been affected by the Medtronic recall of Sprint Fidelis leads.


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Copyright 2009 - 2010 Fields Law Firm a Medtronic Lead Recall Lawyer. Read Our Disclaimer Representing individuals and families related to Medtronic Sprint Fidelis leads, Medtronic defibrillator lead recall and Medtronic lead extractions. Medtronic recall 2010 updates including Sprint Fidelis lead recall, Medtronic lead lawsuit and Sprint Fidelis lawsuit. Medtronic lawsuit and Medtronics recall news and information for Medtronic class action. Serving clients suffering from Medtronic heart defibrillator lead side effects for 6949, 6948, 6931 & 6930 leads in Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, D.C., Delaware, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin and Wyoming.

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