FDA recalls Medtronic Aortic Root Cannulas 

Mar 31, 2025 - 03:12 PM
fda-product-update

The Food and Drug Administration has identified a Class I recall of due to a risk of unexpected loose material in the male luer used in the cannula. The loose material could become dislodged and cause serious injuries or death. The FDA said there have been no reports of injuries or death from the issue. 

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