6930
Medtronic 6930 Recall Sprint Fidelis Lead
It is estimated that 400 Medtronic 6930 leads were implanted in patients in the United States. The Medtronic lead is also referred to as the “Sprint Fidelis 6930″ heart lead. In October 2007 the 6930 lead was recalled following reports of lead fractures. The leads (wires) connect a defibrillator to the heart by placing the leads in or on the heart muscle. The recalled Medtronic leads, including the Medtronic 6930 model, were only used to deliver therapy in defibrillators and they were not used with pacemakers. A fractured lead can cause the implanted defibrillator to either deliver inappropriate shocks or not deliver shocks when needed.
Sprint Fidelis 6930 Lead Fractures
Even though the recalled Medtronic leads are more likely to fracture, it doesn’t mean that every lead will break. However, when a lead does break, the lead can send false signals that cause unnecessary shocks or in the alternative packing or shock therapy many not be delivered when needed.
It is also important to point out that the recalled Medtronic Sprint Fidelis 6930 leads were not only implanted in patients with Medtronic defibrillators. The leads were also used with defibrillators from other manufacturers such as St. Jude and Boston Scientific/Guidant. It is important to check your patient wallet card to identify which lead was implanted.
FDA Patient Recommendations
What should patients do if they have had a Medtronic Sprint Fidelis 6930 lead implanted?
• Patients who have had the Sprint Fidelis lead implanted should contact their physician, especially if they have experienced multiple shocks, lightheadedness, fainting, or palpitations.
• Patients should not routinely seek removal of the device. The risks of removal in most patients exceed the small risk of lead fractures. Therefore, it is generally recommended to leave functioning leads in place. There are two alternatives to removing the lead. One is to continue using the lead while monitoring closely for signs of fracture. A second is to surgically add a replacement lead. Adding a replacement lead does not require removing the 6930 Medtronic lead. If the Sprint Fidelis is left in a patient without being used, it must be “capped”, which means covering the tip with a small plastic insulation.
Medtronic Recall Lawsuit 6930
We represent all Medtronic recall clients with implanted 6930 leads on a contingency basis which means that there are never any legal fees unless we win compensation in your case. For a free no-obligation consultation please call Toll Free at 1-888-343-5375 or fill out our short online contact form and an attorney will contact you to answer any of your questions.
We are a law firm dedicated to helping those injured by Medtronic Sprint Fidelis Defibrillator Lead.
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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, [...]
