Faulty Symmetry Bypass Aortic Connectors

Case ID: 3300 | Drugs / Medical | 04/12/2004
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Have you or a loved one received a St. Jude Symmetry Bypass Aortic Connector?

St. Jude Symmetry Bypass Aortic Connector Comes Under Scrutiny Because of Numerous Complications

Kahn Gauthier Swick is investigating claims that the St. Jude Symmetry Bypass Aortic Connector has been associated with a high occurrence of heart attacks, respiratory failure, and has been linked several deaths. The adverse effects associated with the St. Jude Symmetry Bypass Aortic Connector include graft narrowing, valve leakage, failed deployment, and occlusion. If you or a loved one has received a St. Jude Symmetry Bypass Aortic Connector, please contact a lawyer at Kahn Gauthier for more information.

Despite adverse reports, the manufacturer of the symmetric bypass aortic connector, St. Jude Medical, neither conducted clinical trials or testing of a larger segment of the post-cardiac bypass population, nor have they made any alterations in design or manufacture that would lessen the great danger the symmetry bypass aortic connector poses to implant patients.

Kahn Gauthier Swick intends to pursue litigation of disability and death cases on behalf of symmetric bypass aortic connector device patients whose disability or death were caused by failed a symmetry bypass aortic connector. If you are interested in discussing a potential case and exploring you legal rights, please contact us.


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