Medtronic: Medtronic recalls aortic root devices

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 recall, identified as the FDA's most serious, affects the DLP Aortic Root Cannula, MiAR Cannula and DLP Aortic Root Cannula with Vent [...] The post Medtronic recalls aortic root devices appeared first on Becker's Hospital Review | Healthcare News & Analysis.