FDAFebruary 21, 2025device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Medline medical procedure kits, containing Medtronic Aortic Root Cannula

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lp northfieldmedlinemedline industries

UPCs

101953274496504019532744965110198459089503401984590895041019532749036240195327490363101953274903554019532749035610195327298258401953272982591019532704757340195327047574

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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