FDAFebruary 21, 2025device

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

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

1019532756356140195327563562

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF — Recall Details · AllClear