Medline recalls specific blood culture kits due to expired Bactec components not listed on kit inserts. Users must check expiration dates to avoid potential risks from expired materials.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Medline is recalling certain blood culture kits because they may contain expired Bact:ec components that weren't listed on the kit's instructions. This could lead to inaccurate test results or other issues if the expired components are used.
The kits may include expired Bactec components that weren't listed on the kit's instructions. If the user doesn't check the expiration date of the Bactec inside the kit, they might use expired components, which could lead to inaccurate test results.
Healthcare professionals and labs using the recalled blood culture kits. Those who use the kits without checking the Bactec expiration date are at risk of inaccurate test results.
Check for the reorder number DYNDH1714A and lot number 23KBC138 on the kit's packaging. The kits have a unique identifier: case 40195327347551 and unit 10195327347550.
Inspect the Bactec component inside the kit for its expiration date. If expired, do not use the kit.
The recall is due to expired Bactec components not being listed on the kit's instructions, which could lead to inaccurate test results if used.
Look for the reorder number DYNDH1714A and lot number 23KBC138 on the kit's packaging. The kits have unique identifiers: case 40195327347551 and unit 10195327347550.
Check the Bactec expiration date inside the kit. If expired, do not use the kit and contact Medline for further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0965-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-0965-2024 from Medline. 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.
