Medline recalls CV I II kits with specific lot numbers due to incorrect labeling of model 30001 as 30000. Affected kits may have safety risks if used without proper identification.
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 CV I II kits that were incorrectly labeled as model 30000 instead of 30001 during manufacturing. This labeling error could lead to using the wrong model, which might cause safety issues if the kit is not properly identified.
During manufacturing, the kits were incorrectly labeled as model 30000 instead of model 30001. This labeling error could lead to using the wrong model, which might cause safety issues if the kit is not properly identified for medical use.
Users of Medline CV I II kits with lot number 24ABA223 are affected. Healthcare professionals using these kits for medical procedures may be at risk if they rely on the incorrect model identification.
Check for lot number 24ABA223 on the kit. The kits are labeled with UDI/DI numbers 40195327227235 (case) and 10195327227234 (each).
Look for the lot number 24ABA223 on the kit's label to confirm if it is affected.
The kits were incorrectly labeled as model 30000 instead of model 30001 during manufacturing, which could lead to using the wrong model.
Check the kit's label for lot number 24ABA223. If it matches, contact Medline for further instructions.
The recall is due to a labeling error, not an immediate safety hazard. However, using the wrong model could cause issues in medical procedures.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0123-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0123-2025 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.
