Medtronic Sprint Fidelis Defibrillator

Medtronic, the largest manufacturer of implanted heart devices in the United States, is urging all of the approximately 268,000 patients worldwide (172,000 in the U.S.) with Sprint Fidelis leads, to immediately see their doctors to find out if the wire has fractured. The Sprint Fidelis wire has been used with Medtronic defibrillators since 2004.

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Symptoms Associated with Defective Leads:

The FDA advises patients who have had the Sprint Fidelis lead implanted to contact their doctors, especially if they have experienced the following symptoms:

  • Multiple shocks
  • Lightheadedness
  • Fainting
  • Heart palpitations

Additional Side Effects

Additionally, women have experienced side effects including severe pain and crampingblood clotsinfectionpelvic pain, depressionweight gain, and extreme fatigue. From 2002-2013, the FDA received approximately 988 reports citing adverse events related to Essure.

Contact an Essure Lawyer

Our team of product liability attorneys are experienced in successfully representing women nationwide in cases involving dangerous pharmaceuticals and defective medical device injuries, including transvaginal mesh, Yaz, and Mirena.

If you or someone you love has received an implanted Medtronic defibrillator with Sprint Fidelis leads, call Schuerger Shunnarah Personal Injury Attorneys today at (833) 692-5038.

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Once they’re on our team, we capitalize on their insider knowledge to fight the very insurance executives they used to work for.

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Contact us now and learn your rights and get advice from an attorney who is on your side and knows how the insurance company game is played. 

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