FDA-Device2025-04-16Class I
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF
MEDLINE INDUSTRIES, LP - Northfield
Hazard
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.
Sold states
US: CA, FL, MN, NY, OH, OR, PA, TX, WV
Affected count
320 units
Manufactured in
3 Lakes Dr, N/A, Northfield, IL, United States
Products
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1458-2025Don't want to check this manually?
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