Medline Industries recalls peripheral blood culture draw kits with expired components. Items may not function correctly due to expired materials. Contact for details.
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 certain peripheral blood culture draw kits because some components have expired before the kit's overall expiration date. Using these kits could lead to inaccurate test results or improper blood collection.
The kit components have expired before the overall kit expiration date. This could cause inaccurate blood culture results or improper blood collection during medical procedures.
Healthcare professionals using the recalled Medline Peripheral Blood Culture Draw kits with specific lot numbers are affected. Those handling the kits in clinical settings are most at risk.
Check for lot numbers 23EMF711 or 23CMH027 on the kit's packaging. The product is identified as 'PERIPHERAL BLOOD CULTURE DRAW, REF DYNDH1561' with specific UDI/DI numbers.
Verify the lot number on the kit packaging to confirm if it matches 23EMF711 or 23CMH027.
The recall is due to components within the kit expiring before the overall kit's expiration date listed on the insert.
Check the lot number on the kit packaging. If it matches 23EMF711 or 23CMH027, contact Medline Industries for instructions.
Using expired components could lead to inaccurate blood culture results or improper blood collection, but the risk is low.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0311-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0311-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
