Medline recalls specific Heart CABG CDS kits (model : 30001) with incorrect labeling that could lead to confusion during surgery. Affected kits have lot numbers 24BMF012 and 24CMG491.
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Medline is recalling certain Heart CABG CDS kits that were incorrectly labeled as model 30000 instead of 30001 during manufacturing. This labeling error could cause confusion in surgical settings, potentially leading to incorrect use of the device.
The kits were incorrectly labeled as model 30000 instead of model 30001 during manufacturing. This labeling error could lead to confusion in surgical settings, where using the wrong model might affect device compatibility or procedure safety.
Healthcare professionals using Medline Heart CABG CDS kits with lot numbers 24BMF012 or 24CMG491 are most at risk. These kits were manufactured for model 30001 but labeled as model 30000.
Check the lot numbers on the kit: 24BMF012 or 24CMG491. The kits are labeled as model 30000 but were intended for model 30001.
Look for lot numbers 24BMF012 or 24CMG491 on the kit packaging.
The kits were incorrectly labeled as model 30000 instead of model 30001 during manufacturing, which could cause confusion in surgical settings.
Check the lot numbers on the kit. If it has lot numbers 24BMF012 or 24CMG491, contact Medline for further instructions.
The recall is due to a labeling error, not a safety hazard. There is no risk of injury from using the kit correctly.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0119-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0119-2025 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.
