Medline recalls medical procedure kits with Medtronic Aortic Root Cannula due to potential excess material in male lures. Affected kits have specific labels and lot numbers. Consumers should contact Medline for details.
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.
Medline is recalling medical procedure kits that include Medtronic Aortic Root Cannula because of a potential excess material in the male lures. This could cause issues during medical procedures if not properly managed.
The recall is due to potential excess material in the male lures of the aortic cannula. This could lead to complications during medical procedures if the material causes improper function or blockage.
Medical professionals using these kits are most at risk. Patients undergoing procedures with these kits may also be affected.
Check for the label 'TOL DR R PACK' on the kit. Lot numbers include 22GBL197, 22JBG283, 23ABO787, 23EBT153, 23HBB950, 24CBL126, 24EBV315, 24EBW136.
Look for the label 'TOL DR R PACK' on the medical procedure kit.
The recall is due to potential excess material in the male lures of the aortic cannula, which could cause complications during medical procedures.
Check for the label 'TOL DR R PACK' and lot numbers 22GBL197, 22JBG283, 23ABO787, 23EBT153, 23HBB950, 24CBL126, 24EBV315, or 24EBW136.
The recall record does not specify a remedy, so contact Medline directly for instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1457-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1457-2025 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.