Schmidt & Clark, LLP | A National Law Firm

FDA Video: Recall of Sprint Fidelis Cardiac Leads

Medtronic Inc. has stopped distributing Sprint Fidelis defibrillation leads because of the possibility that these leads could fracture in a small percentage of patients. Included below is a video issued from the FDA regarding the Sprint Fidelis recall.

Medtronic Inc. has stopped distributing Sprint Fidelis defibrillation leads because of the possibility that these leads could fracture in a small percentage of patients.

Although the leads continue to function properly in the vast majority of patients, if one does fracture, the defibrillator could deliver unnecessary shocks or not operate at all. Some deaths and major complications have occurred when the leads fractured.

The affected products are Sprint Fidelis Models 6930, 6931, 6948, and 6949. They are used with implantable cardioverter-defibrillators (ICD) or cardiac resynchronization therapy defibrillators (CRT-D).

Medtronic is advising physicians to stop implanting the leads and to return unused leads to the company. FDA and Medtronic are not recommending prophylactic removal of the leads in most patients, because the risk of removing the lead exceeds the small risk of a fracture.

In addition, the company recommends reprogramming the device to monitor the patient more effectively for potential problems, and to provide an audible alert if a lead does fracture.

Patients who have the Sprint Fidelis lead should contact their physician, especially if they have experienced multiple shocks, lightheadedness, fainting, or palpitations. Patients should also recognize that a small number of Sprint Fidelis leads are used with defibrillators made by manufacturers other than Medtronic. If patients think they have a Sprint Fidelis lead, or if they do not know the model of their lead, they should contact their doctor.

Do I have a Sprint Fidelis Lawsuit?

The Medical Device and Product Liability Litigation Group at our law firm is an experienced team of trial lawyers that focus exclusively on the representation of plaintiffs in Sprint Fidelis lawsuits. We are pursuing individual litigation nationwide and currently accepting new Sprint Fidelis defibrillator lead cases in all 50 states.

If you or a loved one have been injured by the Sprint Fidelis Lead, you should contact us immediately. You may be entitled to compensation and we can help.

Related Content on our Website

Attention Attorneys:  Schmidt & Clark considers a referral from another law firm to be one of the greatest compliments. Our law firm has built a reputation for succsess and accepts a number of case referrals on a regular basis. We do not publish prior verdicts or settlements on our website. If you would like to refer us a case or for us to send you a profile of prior award judgments or average referral fees, please visit the attorney referral section of our website.

Spread the Word ...

If you feel that your family, friends or colleagues would find this page helpful, please share it with them via Facebook, MySpace, Twitter or any of the other popular social networking and/or social bookmarking sites by clicking the button below.

Share/Save/Bookmark

Stay Informed!

If you would like to receive periodic updates regarding new product warnings and recalls, please take a few seconds to sign up for our Email Newsletter or subscribe to our RSS feed.

Toll Free 24 hrs/day (866) 588-0600

Super Lawyers

Million Dollar Advocates Forum

The Best Lawyers in America

Law Dragon 500 - Leading Plaintiff's Lawyers in America


AAJ - American Association for Justice

Lexis Nexis Martindale-Hubbell AV Rating - Peer Review Rated Attorney, Lawyer, Law Firm

People Over Profits

Nationwide Representation - Attorney, Lawyer, Lawsuit, Law Firm, Claim, Case, Suit, Class Action