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Vascular Cannula Recall: Medtronic Removes Aortic Root Cannula Due to Unexpected Loose Material in the Male Luer

Medtronic is recalling Aortic Root Cannulas due to the risk for unexpected loose material in the male luer used in the cannula.

The FDA has identified this as a Class I recall, the most serious type of recall. This recall involves removing certain devices from where they are used or sold. This device may cause serious injury or death if you continue to use it. 

Questions?

Customers in the U.S. with questions about this recall should contact their Medtronic field representative or Customer Service at 1-800-854-3570.