In this study we incorporated different types of aortic root motion into fluid-structure interaction (FSI) models representing an ATAA and a healthy aorta to examine their impacts on wall stress and ...

Medtronic has issued a recall for several aortic root cannula devices due to a potential safety risk that could cause loose material to dislodge during use, potentially leading to stroke or death.

The Food and Drug Administration has identified a Class I recall of Medtronic Aortic Root Cannulas due to a risk of unexpected loose material in the male luer used in the cannula. The loose material ...