Medical Device Recall: Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC CABG, CARDIAC PACK, DR D AC PACK, HEART BASIN PACK-LF, K OH COMPONENT PACK,
MEDLINE INDUSTRIES, LP - Northfield · February 21, 2025
Reason for Recall
Medline medical procedure kits, containing Medtronic Aortic Root Cannula
Product Description
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: CABG OPNHRT S HSP, CARDIAC CABG, CARDIAC PACK, DR D AC PACK, HEART BASIN PACK-LF, K OH COMPONENT PACK, OPEN HEART ADULT PART 1 CDS, OPEN HEART B PACK-LF, OPEN HEART PACK, Z OPEN HEART.
Distribution
US: CA, FL, MN, NY, OH, OR, PA, TX, WV
States Affected
CA, FL, MN, NY, OH, OR, PA, TX, WV
Quantity Affected
1310 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1456-2025
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.