FDAFebruary 21, 2025device

Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: TOL DR R PACK

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

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lp northfieldmedlinemedline industries

UPCs

101953271663044019532716630510195327273484401953272734851019532750339040195327503391

Recall history

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

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