Medtronic Lawsuits
Sprint Fidelis Lead Recall
The Medtronic class action lawsuits are being handled through what is called multidistrict litigation or “MDL”. Lawsuits involving thousands or tens of thousands of people are frequently referred to as class actions, however they are often in the form of multidistrict litigation.
All of the Medtronic recall cases have been consolidated and transferred to federal court in Minnesota where Medtronic is headquartered. Cases are still pursued individually. This means that individuals affected by the Sprint Fidelis lead recall maintain control over their case. Multidistrict litigation typically only involves discovery matters and cases are returned to the original court in which they were filed after the completion of the discovery stage of the Medtronic litigation.
There is not one trial that involves all of the cases. Multidistrict litigation only pertains to the discovery part of the Medtronic lawsuit. Our Medtronic recall attorneys are reviewing individual cases and working with clients throughout the United States. If you would like to discuss your case with a Medtronic lead recall attorney we are ready to help answer your questions. Please call us for a free consultation toll free at 1-888-343-5375 or 1-612-370-1511 or you can also send us an e-mail using our contact form on this page.
We are a law firm dedicated to helping those injured by Medtronic Sprint Fidelis Defibrillator Lead.
Medtronic Recall Lawsuit
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- Medtronic Lead Lawsuit News | Sprint Fidelis Recall
- Medtronic Lawsuits | Medtronics Defibrillator Lawsuit News
- Medtronic Recall News | Sprint Fidelis Lead Fracture Lawsuit
- Medtronic Paradigm Recall Infusion Sets News | Medtronic Quick Set Recall Lawsuit
- Medtronic Lawsuit | Sprint Fidelis Lead Recall Attorney Lawyer
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- Medtronics Lawsuits News | Recalled Sprint Fidelis Heart Leads Attorney Lawyer
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.
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, [...]
In July 2009 the FDA announced a Medtronic Paradigm recall for an estimated 3 million infusion sets used with the Medtronic insulin pump. The Medtronic Quick Set Recall of the infusion sets followed concerns that approximately 60,000 Quick-Set infusion sets used with the Medtronic Paradigm insulin pumps may be defective.
Medtronic Recall Infusion Sets
Medtronic, Inc. and [...]
Patients and families have continued to look at their options of filing a Medtronic lawsuit following the 2007 Sprint Fidelis lead recall. Defibrillator lead fractures have caused heart patients to suffer unnecessary shocks and subsequent surgeries to replace defective leads.
How The Heart Works
For anyone with heart disease, it is important to have as much information [...]
