Sprint Fidelis Recall
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Sprint Fidelis Recall
Why is the Sprint Fidelis ® being recalled?
The Sprint Fidelis ® has been recalled because for lead fractures. The wires are susceptible to breaking or fracturing. This can cause defibrillator to not operate at all or deliver a electric shock.
Five deaths have been reported in relation to this Sprint Fidelis ® defect. Many other serious injuries have also been reported where a faulty lead may have been the cause.
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
The Sprint Fidelis Lead may have also been used to connect defibrillators manufactured by other companies such as Guidant, Boston Scientific, and St. Jude.
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.
