Call Toll free 1-800-231-8857

Best  Sprint Fidelis Implantable Cardiac Lead Device
Attorneys in New York

Sprint Fidelis Implantable Cardiac Lead Device

Important recall notice

On October 15th, 2007, Medtronic, the world’s leading maker
of implantable heart devices, advised the FDA of a voluntary
recall of its Sprint Fidelis defibrillation leads.
It is advised that you see your physician as soon as possible. If
your lead is recommended for removal or replacement you
may be entitled to compensation by the manufacturer. Contact
us at no charge to learn your legal options.
Known Affected Model(s) # 6930, 6931, 6948 & 6949
Our affiliated firms are investigating claims and numerous
adverse event reports made to the FDA arising from failures of
the Sprint Fidelis Implantable Cardiac Lead, a medical device
manufactured by Medtronic, Inc., and its subsidiary, Medtronic
Puerto Rico, Incorporated. These devices are wires that
connect implantable cardiac defibrillators and
resynchronization devices to the heart. The Sprint Fidelis Lead
may have been used to connect devices manufacturer by other
companies such as Guidant, Boston Scientific, and St. Jude,
as well as, Medtronic’s’ own devices. If you have been advised
that your ICD lead must be replaced check your device
identification card to determine if it is a Medtronic Sprint Fidelis
Lead. If so, you may contact us at no charge to discuss your
situation.
When a wire lead is broken or fractured it may cause false or
unnecessary electrical shocks to the heart that could cause
irregular cardiac rhythms that may result in a heart attack or
death.
 
 
 
PleaseGetMeAnAttorney.com can help you find an
experienced Sprint Fidelis Attorney.  We have the best
Sprint Fidelis Attorneys in New York.
 
(please fill out the form to the right)
 
Call Toll free 1-800-231-8857