Medline recalls medical procedure kits containing Medtronic Aortic Root Cannula with specific labels and lot numbers. These kits may pose a risk during surgical procedures.
Medline medical procedure kits, containing Medtronic Aortic Root Cannula
Medline is recalling medical procedure kits that include Medtronic Aortic Root Cannula. These kits have specific labels and lot numbers that could pose a risk during surgical procedures.
The recall does not specify the exact hazard mechanism. The record mentions the product but does not describe how it could be dangerous or what the risk entails.
Healthcare professionals and hospitals that use these kits for cardiac surgery procedures are most at risk. The recall affects specific models and lot numbers.
Check for kits labeled 'CABG OPNHRT S HSP' with specific lot numbers like 23IBH906, 24EBC446, or 24FMC989. The kits may also have UDI/DI codes such as 10195327449650.
Look for the label 'CABG OPNHRT S HSP' and specific lot numbers listed in the recall notice.
The recall does not specify the exact hazard mechanism. The official notice mentions the product but does not describe how it could be dangerous.
Lot numbers 23IBH906, 24EBC446, 24FMC989, 24GME639, 24KMB217, 25AMG162, and others as listed in the recall notice.
The recall does not specify a remedy or action to take, so there is no instruction to stop using the kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1456-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1456-2025 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.
