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Medtronic Defibrillator News
FDA warns Medtronic over external defibrillator
The West Virginia Record - November 23, 2007
By Cara Bailey -Kanawha Bureau

CHARLESTON - A class action lawsuit has been filed against the manufacturers of a heart defibrillator, who claim at least five people have died from lead fractures in the device. The suit seeks $5 million for each member of the class.

FDA warns Medtronic over external defibrillator
Reuters - June 21, 2005
By Susan Heavey

WASHINGTON (Reuters) - Medtronic Inc. failed to properly investigate and correct faulty cable connections with its Lifepak 12 external heart defibrillator, U.S. regulators warned in a letter made public on Tuesday.

FDA: Medtronic didn't fix defibrillator flaws
Star Tribune - June 22, 2005
By Janet Moore

Federal regulators claim that Medtronic Inc. failed to correct manufacturing problems and properly investigate complaints related to a model of external defibrillator commonly found in hospitals nationwide.

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