MEDLINE recalls blood culture kits with incorrect expiration dates on CHG solution and Bactec bottles. This could lead to improper use of the kit. Consumers should check their kit's lot numbers 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 blood culture kits that have incorrect expiration dates on key components. This could lead to improper use of the kit during medical procedures if the expiration date is not followed correctly.
The kit contains a CHG solution and Bactec bottle with expiration dates that don't match the kit's label. This could lead to improper use of the kit during medical procedures if the expiration date is not followed correctly.
Patients and healthcare providers who use MEDLINE blood culture kits with lot numbers 22GME974 or 22FMF309 are affected. Those using the kits for medical procedures are at the highest risk.
Check the kit's lot numbers: 22GME974 or 22FMF309. The product was sold with reorder number DYNDH1592.
Look for lot numbers 22GME974 or 22FMF309 on the kit's packaging.
The kit has an incorrect expiration date on the CHG solution and Bactec bottle, which could lead to improper use during medical procedures.
Check the kit's lot numbers. If they match 22GME974 or 22FMF309, contact MEDLINE for further instructions.
The recall is for incorrect expiration dates, which could lead to improper use but does not pose a direct risk of serious injury.
We’ve drafted a message you can send MEDLINE to request your refund or repair — edit it as you like.
Subject: Recall Z-0122-2023 — MEDLINE MEDLINE Hello, I own a MEDLINE that is covered by recall Z-0122-2023 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.
