Endovascular device recalled by the FDA


Zenith Alpha Thoracic Endovascular Graft
August 28, 2017 Categories: Defective Medical Devices

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Endovascular device recalled by the FDA

The FDA issued a safety alert for Zenith Alpha Thoracic Endovascular Graft – a device for the endovascular treatment of patients with aneurysms.
Class I Recall – Potential Formation of Thrombus Inside Device.

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