Medline recalls ADLT Blood Culture Collect Kit (ref DYNDH1245) due to expired components. Affected kits may have expired items before the kit's expiration date.
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 is recalling ADLT Blood Culture Collect Kits with specific lot numbers because some components inside the kit expired before the kit's overall expiration date. This could lead to inaccurate test results if used.
The kit contains components that expired before the kit's expiration date. Using expired components may cause inaccurate blood culture test results, but does not pose a direct health risk to users.
Healthcare professionals using the ADLT Blood Culture Collect Kit for blood tests. Those who have the kit with lot numbers 23EMI373, 2:3EMF712, 23DMF155, or 23CMH026 are most at risk.
Check the kit's lot number on the case (40889942604723) and unit (10889942604722). Affected kits have lot numbers 23EMI373, 23EMF712, 23DMF155, or 23CMH026.
Look for lot numbers 23EMI373, 23EMF712, 23DMF155, or 23CMH026 on the case (40889942604723) or unit (10889942604722).
The kit contains components that expired before the kit's overall expiration date, which could lead to inaccurate blood culture test results.
Check the lot number on the case or unit. If it matches the affected lot numbers, stop using the kit and contact Medline for instructions.
The recall does not provide a fix; affected kits should be discarded or returned to the manufacturer.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0310-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0310-2024 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.
