The Medtronic Sprint Fidelis leads were pulled from the market in October 2007
because fractures had been detected in some wires. There are approximately 268,000 Medtronic leads implanted in patients worldwide. Medtronic’s Sprint Fidelis defibrillation leads were recalled following the reporting of major complications and the death of several heart patients.
Patients have experienced complications as a result of defective leads such as unnecessary shocks or jolts or not operating at all. In their October 15, 2007 letter to patients, Medtronic states that patients with a Sprint Fidelis lead “…are more likely to experience complications from removal than from a problem with a Sprint Fidelis lead”. This puts patients who have experienced problems or side effects in the difficult position of deciding whether to have the Medtronic leads removed or risk potential problems. There is currently no test that will predict if a Medtronic lead will fracture. The FDA advises that defibrillator settings be adjusted so that potential fractures can more easily be detected in patients.
Implantable cardioverter defibrillators (ICDs) and Cardiac Resynchronization Therapy-Defibrillators (CRT-Ds) are used to treat abnormal heart rhythms that can cause the heart to suddenly stop. Implanted defibrillators shock the heart back into normal rhythm by sending an energy pulse through an electronic lead (wire) that is connected to the patient’s heart.
If you or a loved one has been injured by a defective Medtronic defibrillator lead please contact us for a free consultation and case review. A Medtronic class action lead attorney can go over your legal rights and options and evaluate any potential claims you may have. You may be entitled to compensation and we can help.
We are a law firm dedicated to helping those injured by Medtronic Sprint Fidelis Defibrillator Lead.
Medtronic Recall Lawsuit
U.S. Food & Drug Administration Statement On Medtronic Sprint Fidelis Defibrillator
Medtronic Suspends Sprint Fidelis Defibrillation Leads (PDF)
U.S. FDA Class 1 Recall Report
If you or a loved one have been injured by the Medtronic Sprint Fidelis lead please contact us immediately. You may be entitled to compensation.
Medtronic lawsuits continue to be filed on behalf of patients affected by the Sprint Fidelis Medtronics recall. Implantable Cardioverter-Defibrillators (ICDs) are implanted heart devices that shock dangerous abnormal heart rhythms back to a normal rhythm. The lead is a wire that connects the ICD to the heart. Medtronic, Inc., a Fortune 500 company based in [...]
Since the Medtronic recall of Sprint Fidelis heart leads in October 2007, patients are continuing to suffer from the life threatening consequences of a fractured defibrillator lead with no real legal recourse. Following the 2008 Supreme Court decision Riegel v. Medtronic, patients and families have been prevented from having the right to file a viable [...]
Sprint Fidelis leads are manufactured by Medtronic, the medical device manufacturer headquartered in Minnesota. The Medtronic Fidelis lead consists of cardiac electrodes which are thin wires. These electrodes connect an implantable cardioverter-defibrillator (ICD) or cardiac resynchronization therapy defibrillator (CRT-D) to the heart.
The Medtronic Fidelis leads recall was announced by the manufacturer and the FDA due [...]
This Medtronic lawsuit center website provides information about the Sprint Fidelis Medtronic Lawsuits nationwide. Below is a Medtronic Lead Recall and Judicial Directory for Mississippi through Wyoming. If you or a loved one has suffered from a defective Medtronic lead, you have a limited period of time to file a claim. Call 1-888-343-5375 for a free, [...]
This Medtronic lead recall center website provides information about the Sprint Fidelis Medtronic Lawsuits nationwide. Below is a Medtronic Recall and Judicial Directory for Alabama through Minnesota. If you or a loved one has suffered from a defective Medtronic lead, you have a limited period of time to file a claim. Call 1-888-343-5375 for a free, [...]