Minn. judge dismisses Medtronic heart device suits
-Reuters
10/28/2009 - A Minnesota state court judge has dismissed a batch of lawsuits against Medtronic Inc stemming from the October 2007 recall of the medical device maker's Sprint Fidelis defibrillator leads.
Minnesota District Court Judge Denise Reilly last week granted a motion by Medtronic to dismiss 600 separate personal injury claims related to use of the leads, which connect an implantable cardioverter defibrillator to a patient's heart and are the conduit for the electricity used to shock the heart back into normal rhythm.
The judge ruled the claims are preempted under federal law, according to court papers.
In January, a U.S. district court judge dismissed a group of federal cases consolidated in Minnesota, citing the U.S. Supreme Court's 2008 Riegel v. Medtronic ruling that reaffirmed the U.S. Food and Drug Administration approval process for determining the safety and effectiveness of medical devices.
A bill pending in Congress, called the Medical Device Safety Act, could repeal the FDA's preemption authority and nullify the Supreme Court's Riegel decision if passed.
Medtronic recalled the Sprint Fidelis line of leads in 2007 after several patients died, possibly because their leads had fractured. The Minneapolis-based company, the largest maker of ICDs to treat abnormal heart rhythms, later said as many as 13 deaths may have been linked to the leads.
The case is In re Medtronic Sprint Fidelis Lead Products Liability State Court Litigation, District Court, Fourth Judicial District, County of Hennepin, State of Minnesota, No. 27-CV-07-22446.
If you or a loved one have had the device replaced or plan to have it replaced you may be entitled to compensation regardless if you suffered as a result of complications from surgery or the device itself. Contact the Medtronic attorneys of Ennis & Ennis today for a free confidential case evaluation. Our on staff nurse and lawyers are standing by to answer any questions you may have regarding the Medtronic pacemaker defects, a possible Medtronic class action lawsuit, or any other type of Medtronic Pacemaker litigation.
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