Medline Industries recalls 24-Blood Culture Kits with expired components that could lead to infection if used after expiration. Affected kits have specific lot numbers and were sold in 2023.
This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
Medline Industries is recalling 24-Blood Culture Kits that contain expired components. Using these kits after the expiration date could lead to infection risks.
The kits contain components that have expired before the overall kit expiration date. Using expired components could lead to infection risks if the kit is used after the expiration date.
Healthcare professionals and labs using the recalled kits are most at risk. Patients using these kits for blood tests may face infection risks if the expired components are used.
Check for lot numbers 23EMF710, 2:3DMF154, or 23DMA779 on the kit's packaging. The kits were sold in 2023 and have specific model numbers.
Verify the kit's expiration date and lot numbers to confirm if it is affected.
The kit contains components that have expired before the overall kit expiration date listed on the insert.
Lot numbers 23EMF710, 23DMF154, and 23DMA779.
Check the lot numbers on the kit's packaging; affected kits have lot numbers 23EMF710, 23DMF154, or 23DMA779.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0313-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0313-2024 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.