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Drugs & Medical Devices Medtronic Sprint Fidelis Recall Research Center

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in this section: Recalled Model Numbers | Medtronic lawsuit information | Recall Notice | Ventricular Fibrillation | Sudden Cardiac Death | Electrophysiology | Medtronic Cardiac Innervation | Ischaemic Myocardium | History

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NEW RECALL: Medtronic's Sprint Fidelis Leads (used with implantable defibrillators)

Were Medtronic Inc's Sprint Fidelis leads used to attach your defibrillator to your heart?

Medtronic, Inc. has issued a recall of its Sprint Fidelis leads due to a flaw whereby they could break or erode.

The FDA explained, "In the infrequent circumstance where a lead actually breaks, or 'fractures,' the lead may send false signals that cause inappropriate defibrillator shocks, or therapies such as pacing or shocks may not be delivered."

In view of this recall, you should find out whether Medtronic's Sprint Fidelis leads were used to implant your defibrillator?

Weitz & Luxenberg is currently representing men and women who have been seriously injured by the recalled Medtronic Sprint Fidelis Models: 6930, 6931, 6948, and 6949. Learn more about our Medtronic practice. Time may be running out to file your suit. Complete the form below to get started.

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Please complete the following questionnaire:

Name
Email
Phone Number
Were you implanted with a Medtronic Sprint Fidelis Lead?
If yes, when?
Has your defibrillator failed to work?
If yes, please describe failure
Has your Medtronic Sprint Fidelis Lead been replaced?
If yes, when?
Additional comments


see also:

Sudden Cardiac Death Sudden Cardiac Death - Information Regarding Faulty Medtronic Leads
Sudden Cardiac Death and Medtronic Defibrillators

Ischaemic Myocardium Ischaemic Myocardium & Medtronic's recalled leads: Have You Been Hurt?
Ischaemic Myocardium Medtronic Defibrillator: Do you need a lawyer?

News & Warnings Read the latest news on the Medtronic Defibrillator Recall
Do you have a defibrillator with Medtronic leads? Get the recall news!
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