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Medtronic Sprint Fidelis Leads

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Dangerous faulty wires from Sprint prompt nationwide Medtronic recall

Weitz & Luxenberg is no longer taking Medtronic Cases

Medtronic Inc. has issued a voluntary recall of its Sprint Fidelis leads. The Medtronic recall was issued because the manufacturer's lead wires that connect implantable defibrillators to the heart, can potentially break or erode, raising the possibility of injury.

Just prior to the Medtronic recall, the FDA issued a statement confirming that, "some deaths and major complications have occurred," as a result of these faulty leads.

The lawyers of Weitz & Luxenberg currently represent many individuals who were injured prior to the Medtronic recall, as well as after the Medtronic recall. These clients were implanted with defective Medtronic Sprint Fidelis leads numbered: 6930, 6931, 6948, and 6949.

Representing New York's largest personal injury law firm, Weitz & Luxenberg attorneys responded to the Medtronic recall by beginning procedures to hold Medtronic accountable for endangering people's lives with these faulty medical devices, and seeing that they are well compensated for their injuries and suffering.

The first step towards filing your Medtronic recall lawsuit begins by completing the Medtronic recall form on this page. Tell us your story and a representative from our firm will be in touch shortly.


see also:

Press Release Breaking News: Weitz & Luxenberg Responds to Medtronic Device Recall
Leading Firm Responds to News of Faulty Medtronic Sprint Fidelis Leads

Removal Report about Surgical Removal of Failed Medtronic Leads: Drug Lawyer
Patients may face risky surgical procedures to remove Medtronic cable

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A nationally-recognized personal injury law firm, Weitz & Luxenberg is committed to helping clients win cases, get the compensation to which they’re entitled and continue with their lives. In just over 20 years, we’ve collected more than $1.3 billion for plaintiffs.