Medline Industries recalls specific Open Heart Nimc Kits due to incorrect labeling during manufacturing, potentially causing confusion with different model numbers.
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 Industries is recalling certain Open Heart Nimc Kits that were incorrectly labeled as model 30000 instead of model 30: This could lead to using the wrong kit in medical procedures. The recall affects kits with specific lot numbers and model identifiers.
During manufacturing, the kits were incorrectly labeled as model 30000 instead of model 30001. This labeling error could lead to confusion between different kit models, potentially causing incorrect use in medical procedures.
Medical professionals using the recalled kits are most at risk, particularly those who might use the wrong model in critical procedures. The recall applies to specific kits sold with lot number 24BMF235.
Check for the lot number 24BMF235 on the kit packaging. The kits have a unique identifier: UDI/DI 40195327185078 (case) or 10195327185077 (each).
Look for the lot number 24BMF235 on the kit packaging to confirm if it is affected.
The recall affects kits that were incorrectly labeled as model 30000 instead of model 30001.
Check for the lot number 24BMF235 on the kit packaging. The kits have a unique identifier: UDI/DI 40195327185078 (case) or 10195327185077 (each).
The recall record does not specify a remedy, so no action is required beyond checking the kit label.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0124-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0124-2025 from Medline Industries. 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.
