Medline recalls medical procedure kits containing Medtronic Aortic Root Cannula due to potential excess material in male lures. Affected kits have specific lot numbers and UDI/DI codes. 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 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.
Healthcare professionals using these kits in medical procedures are most at risk. Patients receiving these procedures may be affected if the kits are used without proper checks.
Check for kits labeled 'CPB ADJUNCT PACK, DR. C' with specific lot numbers and UDI/DI codes listed in the recall notice. The kits include details like lot numbers 24IBV027, 22HBX339, and other identifiers.
Reach out to Medline Industries for specific details about your kit and instructions on what to do next.
The recall states potential excess material in the male lures of the Medtronic Aortic Root Cannula, which could cause complications during medical procedures.
Check for kits labeled 'CPB ADJUNCT PACK, DR. C' with specific lot numbers and UDI/DI codes listed in the recall notice.
Contact Medline Industries directly for details on your specific kit and instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1459-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1459-2025 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.
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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.
