Medtronic 6948 Lead Fractures | Fidelis 6948 Recall Lawsuit
If you or someone you know has received a Medtronic 6948 defibrillator lead you may have important legal rights. Many heart patients have experienced a lead fracture which can cause painful and sometimes life-threatening shocks to the heart or alternatively not provide a shock when needed. We are currently representing patients who have defective Medtronic 6948 leads in filing individual Medtronic recall lawsuits.
Following the death of five patients Medtronic removed its Sprint Fidelis 6948 lead along with models: 6930, 6931 and 6949. A lead fracture in the defibrillator wire can cause serious problems by either sending an unnecessary jolt to the hart or not operating at all.
Medtronic 6948 Lead
U.S. Market Release September 2004
Serial Number Prefix LFH
Type and/or Fixation Transvenous, Vent, Defib and Pace/Sense, Tines
Polarity True Bipolar / Two Coils
Steroid Yes
Estimated U.S. Implants 10,700
Estimated U.S. Active 8,700
Fields Law Firm is a Minneapolis, Minnesota based law firm that is working with patients affected by the Medtronic 6948 recall throughout the United States.
We represent all Medtronic recall clients 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 a Medtronic recall 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.
Patients subject to the Sprint Fidelis recall continue to suffer from a Medtronic lead failure leading to a surgery to replace the defective lead. The Multidistrict Medtronics lawsuit is currently under appeal and lawyers representing victims are continuing to fight for the right to bring a claim for compensation.
If you have been diagnosed with an [...]
In January 2009 the United States District Court ruled the Sprint Fidelis Medtronic Lawsuit Dismissed. This ruling is currently under appeal and attorneys representing patients and families affected by the Medtronic recall continue to fight for their rights. The Medtronics recall involves only the Sprint Fidelis lead and not the implanted heart device.
The defibrillator lead [...]
The Medtronic lead lawsuit Multidistrict litigation continue even though there have been setbacks and we continue to push for the Medical Device Safety Act legislation which will help protect patients with medical devices. The Sprint Fidelis recall failure rate of defibrillator leads continues to leave heart patients in the difficult position of not knowing if [...]
It is estimated there are 150,000 heart patients throughout the United States affected by the Medtronic lead recall who have a recalled defibrillator lead wire and are at risk of a lead fracture. Medtronic lawsuits continue to be filed on behalf of patients who have suffered a lead fracture. The Medtronic Sprint Fidelis leads were [...]
Patients continue to suffer from a Medtronic Sprint Fidelis lead fracture following the 2007 Medtronic recall of defibrillator leads. If you or a loved one has suffered from fractured leads please contact us today for a free consultation and information how we can help.
What is a Defibrillator?
We’ve seen them used on the TV hospital programs, [...]
