Medtronic lead recall information video

The December 2007 FDA Patient Safety News show contains a segment highlighting the Medtronic lead recall, which has impacted 235,000 people with one of the defective wires connecting their defibrillator to the heart.  The lawyers at Saiontz & Kirk, are reviewing Medtronic lead recall lawsuits nationwide for any individuals who have one of the recalled leads, which will be indicated on patient information card with any of the following model numbers: 6930, 6931, 6948 or 6949.

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FDA PATIENT SAFETY NEWS: MEDTRONIC LEAD RECALL VIDEO

The monthly broadcast of the FDA Patient Safety News show contains updates and information about FDA safety notifications and product recalls, as well as information about ways patients can protect themselves when using medical products.

On October 15, 2007, the FDA and Medtronics, Inc. issued a nationwide recall for the Sprint Fidelis Cardiac Defibrillator lead.  The small electrical wires are prone to fracture or break, which could cause unnecessary shock or device failure.

According to initial estimates, approximately 2.3% of all leads implanted suffered problems within 30 months.  This could mean that between 4,000 and 5,000 people could experience problems. 

MEDTRONIC LEAD RECALL LAWSUITS

The lawyers at Saiontz & Kirk, P.A. are investigating potential Medtronic lead recall lawsuits for any individuals who had one of the recalled leads implanted with their defibrillator, even if no problems have been experienced.  Consult with your physician or review you patient information card to determine if you, a friend or family member may have one the recalled leads.

Free consultations and claim evaluations are available to help determine if one of the recalled defibrillator leads were used .  There are no fees or expenses unless a recovery is obtained.  To determine if financial compensation may be available, request a free consultation.