Class I

Medical Device Recall: Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF

MEDLINE INDUSTRIES, LP - Northfield · February 21, 2025

Reason for Recall

Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

Distribution

US: CA, FL, MN, NY, OH, OR, PA, TX, WV

States Affected

CA, FL, MN, NY, OH, OR, PA, TX, WV

Quantity Affected

320 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1458-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.