Medline recalls specific blood culture kits due to expired Bact: risk of using expired components if not checked. Affected kits have lot number 23JBQ525. Contact Medline for details.
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 Bactec components. If users don't check the expiration date on the Bactec inside the kit, they risk using an expired component which could lead to inaccurate test results.
The kits may contain expired Bactec components because the expiration date wasn't properly noted on the kit insert. If users don't check the Bactec's expiration date before use, they could be using an expired component, which might lead to inaccurate test results.
Healthcare professionals and lab staff who use Medline blood culture kits with lot number 23JBQ525 are most at risk. Patients using these kits may also be affected if the test results are inaccurate.
Check for the lot number 23JBQ525 on the kit's case or unit. The kits have reorder number DYNDH1622C and UDI/DI numbers 40195327509874 (case) or 10195327509873 (unit).
Look inside the kit for the Bactec component's expiration date to ensure it hasn't expired.
The recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert, risking use of expired components.
Check for lot number 23JBQ525 on the kit's case or unit, with reorder number DYNDH1622C and UDI/DI numbers 40195327509874 (case) or 10195327509873 (unit).
Check the Bactec component's expiration date before use. If expired, 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-0968-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-0968-2024 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.
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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.
