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Lawyers Help Out Medtronic victims in getting Medtronic Recall Lawsuit
The Johnson Law Firm Medtronic lawyers provide the latest information on the litigation involving defective medical devices for victims of these drugs.
By: Johnson Law Firm
“Adequate testing and checking of Medtronic lead by the manufacturer prior to introducing it in market would have revealed the risks with the device and saved many of these patients from additional surgerical expenses, and possibly death,” says a lawyer of Johnson Law Firm.
A recalled Medtronic defibrillator lead is a potentially life threating device for heart patients. The recalled heart leads work in conjunction with a defibrillator and / or pacemaker. Heart lead wires are threaded through veins, connecting the defibrillator / pacemnaker to specific parts of the heart. The lead's failure can cause the defibrillator to either deliver an unnecessary electrical jolt or fail to give an electrical shock to a patient with an abnormal heart rhythm leading to death. Sprint Fidelis lead replacement surgery is required in many cases where the recalled leads have fractured or present this risk. According to FDA, patients who have had the Sprint Fidelis lead implanted should contact their physician, especially if they have experienced multiple shocks, lightheadedness, fainting, or palpitations.
The Johnson Law Firm Medtronic lawyers provide the latest information on the litigation involving defective medical devices for victims of these drugs. Both individual and class action defective Medtronic lead cases from across the country are being reviewed here.
About Johnson Law Firm
The Johnson Law Firm represents clients with defective medical device cases from across the United States. It has established a nationwide claims filing department and information center. Patients can now gather the latest information about FDA Recall, Medtronic Lead Recall frequently asked questions and legal claims against Medtronic at http://www.lawyersforclients.com/