Sprint Fidelis
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Sprint Fidelis
The Sprint Fidelis ® family of defibrillator leads has been recalled. These ICD leads have been linked to reports of at least 5 patient deaths as well as other serious, life-threatening complications.
The Sprint Fidelis ® leads were implanted in approximately 268,000 people. Other companies such as Guidant, Boston Scientific, and St. Jude may also have used the lead to connect defibrillators.
Patients who have had the Sprint Fidelis ® lead implanted should contact their physician immediately, especially if they have experienced;
- Multiple Shocks
- Lightheadedness
- Fainting
- Palpitations
The following model numbers of the Sprint Fidelis ® family of defibrillator leads have been recalled:
- Sprint Fidelis® 6930
- Sprint Fidelis® 6931
- Sprint Fidelis® 6948
- Sprint Fidelis® 6949
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. We can help.
