Medtronic Sprint Fidelis Lead

In of October 2007, the FDA issued a Class I recall of the Medtronic Sprint Fidelis lead due to a flaw that can cause the device to malfunction.  A Class I recall is the most serious type of recall since there is a reasonable chance that the product will cause serious health problems or death. The Sprint Fidelis lead, the thin wire that connects a defibrillator to a patient's heart, can fracture or break which could result in a massive electrical jolt or cause the device not to work at all.  This product was released to the market in 2004.  Any defibrillator implanted since 2004 could have one of the leads. 

The recall applies to the following model numbers:

• Sprint Fidelis Model 6930
• Sprint Fidelis Model 6931
• Sprint Fidelis Model 6948
• Sprint Fidelis Model 6949

There is currently no reliable test to predict whether the Medtronic lead wire will fracture in the future.  Patients should contact their physician immediately if they experience unexpected shocks. Those patients who require the removal of a fractured lead device face a dangerous surgical procedure to replace the defective leads. 

Alley, Clark & Greiwe is one of only a handful of firms that are involved in litigation with Medtronic leads. Please contact our office immediately if you or someone you love has been received a Medtronic Lead that has been recalled.

Topic Video

• View FDA Patient Safety News Video from December 2007

Helpful Consumer Links

• Click here to read March 14, 2009, New York Times article about Medtronic Sprint Fidelis Lead recall
• Click here to view March 13, 2009, "Dear Doctor" Letter from Medtronic
• Click here to read more about recent study that shows Medtronic lead wires failing at higher rates than previously reported.
• Click here for more information regarding Medtronic recall
  
• Click here to view FDA Q&A
  
• Click here to view FDA Class I Recall Notice 
• View FDA Patient Safety News - December 2007