Ennis & Ennis, P.A. is representing individuals that have been harmed as a result of Medtronic defibrillator or pacemaker defects. If you or a loved one have been injured you may be entitled to compensation. For more information about your legal rights or for more information regarding the Medtronic recall click here to contact one of our Medtronic Attorneys about a Medtronic lawsuit today.
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Supreme Court Hears Arguments in Device Preemption Case
-FDA News
12/11/2007 - The Supreme Court heard oral arguments in Riegel v. Medtronic last week and will rule on whether the express preemption provision of the Federal Food, Drug and Cosmetic Act (FDCA) preempts state-law claims seeking damages for injuries caused by medical devices with FDA premarket approval (PMA).
Charles Riegel and his wife sued Medtronic after he was injured when a Medtronic balloon catheter burst during an angioplasty procedure. The Riegels alleged state-law claims for negligent design, testing, inspection, manufacture, distribution, labeling, marketing and sale of the device, as well as strict liability and breach of express and implied warranty.
Medtronic sought summary judgment on grounds of express preemption under the Medical Device Amendments to the FDCA. The district court granted Medtronic’s motion and the U.S. Court of Appeals for the Second Circuit affirmed the ruling.
The outcome of this case is significant for the most technologically sophisticated companies that must use PMA applications for approval rather than 510(k) notifications, James Beck, counsel with law firm Dechert’s product liability group, said.
Ennis & Ennis, P.A. is representing individuals that have been harmed defective medical devices such as the Medtronic defibrillator and pacemaker. If you or a loved one have suffered as a result of a defective Medtronic pacemaker or defibrillator or if you need more information about the Medtronic recall or class action lawsuit click here for a free, confidential case evaluation.
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