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FDA MedWatch


03/18/2008 -  FDA issued a Public Health Notification to inform healthcare professionals of an update to earlier FDA safety information on this product. The notification re-emphasizes the need for continued surveillance of patients treated with endovascular grafts, and provides updated information on the mortality risks associated with the use of the AneuRx Stent Graft System to prevent abdominal aortic aneurysm rupture.

Read the complete MedWatch 2008 safety summary, including a link to the Public Health Notification and previous MedWatch alerts, at:
http://www.fda.gov/medwatch/safety/2008/safety08.htm#AneuRx

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