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Product Liability: Medtronic Sprint Fidelis Lead Wire

Medtronic Sprint Fidelis Heart Lead Wire

THE SIMPLE FACTSTM...On October 15, 2007, Medtronic issued a statement in which it suspended the sale and shipment of its heart lead wire products and requested that all unused heart lead wire products be returned immediately to Medtronic.

The reason for the recall of the Sprint Fidelis heart lead wire products was due to reports of several patient deaths associated with the heart lead wires because the heart lead wires were prone to cracking and potentially life-threatening consequences such as firing repeatedly, unnecessary shocks and/or not sending an electrical jolt when needed.

Some of the warning signs may include:

  1. excessive shocks
  2. lightheadedness
  3. fainting
  4. palpitations

In addition, the Food and Drug Administration (“FDA”) issued a Class 1 recall (the most stringent) of the Medtronic Sprint Fidelis heart lead wires. The recalled Medtronic Sprint Fidelis heart lead wires have been implanted in an estimated 268,000 patients worldwide since late 2004.

The Medtronic Sprint Fidelis heart lead wire is connected to defibrillators or pacemakers either made by Medtronic or by another heart device manufacturer such as Guidant or St. Jude. The Medtronic Sprint Fidelis heart lead wires that are subject to the FDA recall are the following model numbers:

  • 6930
  • 6931
  • 6948
  • 6949

In order to determine if you have one of Medtronic’s Sprint Fidelis heart lead wire products, just review your patient i.d. card and look for the manufacturer name -“Medtronic”- and one of the following numbers – “6949”, “6948”, “6931” and “6930”.


If you experience any problems - lightheadness, palpitations, multiple shocks or fainting - with your heart device, please contact a doctor immediately.


Quite frankly, the simple factsTMabout the problems and side affects possibly associated with the Medtronic’s Sprint Fidelis heart lead wire product are not acceptable.

We are investigating claims of health problems, side effects and problems possibly associated with the use of the Medtronic Sprint Fidelis lead wire.

We are here to help you protect your legal rights and the legal rights of your loved ones.

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It is very important that you work with an experienced personal injury lawyer in order to determine which factors may lead to the possible filing of a formal lawsuit/litigation in connection with a personal injury.

If you or someone you love has one of the recalled Medtronic Sprint Fidelis Lead wires - 6930, 6931, 6948, 6949 - and has experienced any problems with your heart device, please contact us today for a Free Medtronic Lead Wire case evaluation.

Our firm will review your claim without charge or obligation on your part. Alternatively, you may call us toll-free at 1.800.672.4916 to submit your case and contact information for a free case evaluation.

We are here to help you protect your legal rights and the legal rights of your loved ones.




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Updated on July 17, 2009

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