Medtronic Recall Attorney

On October 15, 2007, the U.S. Food and Drug Administration posted the following notice about a Medtronics Recall.

Class 1 Recall: Medtronic Inc. Sprint Fidelis® Defibrillator Leads

Product: Medtronic Inc. Sprint Fidelis® Defibrillator Leads, model numbers 6930, 6931, 6948 and 6949 manufactured from September 2004 through October 15, 2007.

Use: Leads are thin wires that connect an implantable cardioverter defibrillator (ICD) or cardiac resynchronization therapy defibrillator (CRT-D) directly to the heart. ICDs and CRT-Ds are devices that are used to treat abnormal heart rhythms that can cause the heart to stop suddenly.

Recalling Firm:
Medtronic Inc.
7000 Central Avenue
Minneapolis, Minnesota 55432-3576

Reason for Recall: These leads are being recalled because a small number of fractures have been detected. When the lead breaks (fractures), it may cause inappropriate shocks or result in a loss of therapy, such as pacing or shocking.

If you believe you were harmed or adversely affected by the use of the Medtronic Defibrillator Leads, you should contact Ted Machi and Associates, P.C.

Attorneys to Handle Your Medtronic Recall Concerns

Our firm consists of a Arlington-Fort Worth Board Certified* Personal Injury attorney with an experienced team of trial attorneys who are qualified to provide you with excellent representation of your injury claim. Contact an Arlington Texas Personal Injury Lawyer from the firm of Ted Machi and Associates, P.C. today to handle your Medronic issues.

Medtronic Recall

Ted Machi & Associates, P.C., 1521 N. Cooper, Ste. 550, Arlington, Texas
(817) 335-8880 | Metro: (972) 445-5387 | Toll Free: 1 (866) 332-8377
Principle office located in Arlington, Texas

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