MEDLINE recalls adult blood culture kits with incorrect expiration dates on CHG solution and Bactec bottles. This could lead to improper use of the kit if expired components are used. Consumers should check their kit's lot number and contact MEDLINE for details.
Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
MEDLINE is recalling adult blood culture collection kits because they contain an incorrect expiration date on key components. Using expired components could lead to improper blood culture results or infection risks. Affected kits have a specific lot number and were sold with reorder number DYNDH124: 22FMF306.
The kit includes a CHG solution and Bactec bottle that have expiration dates mismatched with the kit's label. Using expired components could lead to inaccurate blood culture results or potential infection risks if the components are not properly stored or used.
Patients and healthcare providers who use MEDLINE adult blood culture kits with lot number 22FMF306 are affected. Those who have the kit and are using it for medical procedures are at risk of improper results if expired components are used.
Check the kit's lot number, which is 22FMF306. The product was sold with reorder number DYNDH1245 and has UDI/DI numbers (01)40889942604723 for the case and (01)10889942604722 for the kit.
Look for the lot number 22FMF306 on the kit's packaging or label.
The recalled kits have lot number 22FMF306.
Check the lot number on the kit's packaging; affected kits have lot number 22FMF306 and were sold with reorder number DYNDH1245.
The recall does not specify a remedy, so contact MEDLINE directly for guidance on next steps.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-0120-2023 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-0120-2023 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.
