Medline recalls Central Line Blood Culture DRA kits with expired components. Items with lot numbers 23DMF156, 23CMH030, or 23CMD955 may have expired components 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 Central Line Blood Culture DRA kits that contain expired components. Using these kits could lead to improper blood culture results due to expired materials.
The kit components have expired before the overall kit expiration date. This could lead to inaccurate blood culture results if the expired components are used in the testing process.
Healthcare professionals using Medline Central Line Blood Culture DRA kits with lot numbers 23DMF156, 23CMH030, or 23CMD955 are affected. Patients receiving blood cultures through these kits may be at risk of inaccurate results.
Check the lot numbers on the kit: 23DMF156, 23CMH030, or 23CMD955. These kits were sold with UDI/DI numbers 40193489402446 (case) and 10193489402445 (unit).
Look for lot numbers 23DMF156, 23CMH030, or 23CMD955 on the kit packaging.
The recall is due to items within the kit having expired prior to the overall kit expiration date listed on the insert.
The official recall notice does not specify a remedy, so contact Medline Industries for guidance.
Check the lot numbers: 23DMF156, 23CMH030, or 23CMD955. These kits were sold with UDI/DI numbers 40193489402446 (case) and 10193489402445 (unit).
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0312-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0312-2024 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.
