Sprint Fidelis Implantable Cardiac Lead Device

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Important recall notice

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On October 15th, 2007, Medtronic, the world’s leading maker of implantable heart devices, advised the FDA of a voluntary recall of its Sprint Fidelis defibrillation leads.

It is advised that you see your physician as soon as possible. If your lead is recomended for removal or replacement you may be entitled to compensation by the manufacturer. Contact us at no charge to learn your legal options.

Known Affected Model(s) # 6930, 6931, 6948 & 6949

Our affiliated firms are investigating claims and numerous adverse event reports made to the FDA arising from failures of the Sprint Fidelis Implantable Cardiac Lead, a medical device manufactured by Medtronic, Inc., and its subsidiary, Medtronic Puerto Rico, Incorporated. These devices are wires that connect implantable cardiac defibrillators and resynchronization devices to the heart. The Sprint Fidelis Lead may have been used to connect devices manufacturer by other companies such as Guidant, Boston Scientific, and St. Jude, as well as, Medtronic’s’ own devices. If you have been advised that your ICD lead must be replaced check your device identification card to determine if it is a Medtronic Sprint Fidelis Lead. If so, you may contact us at no charge to discuss your situation.

When a wire lead is broken or fractured it may cause false or unnecessary electrical shocks to the heart that could cause irregular cardiac rhythms that may result in a heart attack or death.

If you or a loved one has Spint Fidelis device, please fill out our contact form and an experienced DrugSettlement.com attorney or representative will contact you for a free and confidential case evaluation.