TELECTRONICS PACING SYSTEMS, INC. ACCUFIX ATRIAL "J" LEAD PRODUCT LIABILITY LITIGATION

Zimmerman Reed was able to achieve a successful resolution for claims on behalf of patients who had defective pacemakers leads. Zimmerman Reed represented these individuals in a case naming Telectronics Pacing Systems, Inc. and various affiliates, alleging that the company put defective Accufix Atrial Pacemaker "J" Leads on the market. The "J" Lead, which had since been recalled by the Food & Drug Administration, was used in heart surgery to secure a pacemaker to the heart muscle. A fractured "J" wire presents a risk of protrusion of the wire into the heart muscle, resulting in possible, uncontrollable hemorrhage.

If you or a family member has now, or has in the past, received a Telectronics Pacemaker "J" Lead with model numbers 330-801 or 329-701, and you would like more information about pursuing a potential claim, please e-mail our attorneys for more information or call toll-free at 1-800-755-0098.