Remel recalls 100 Blood Agar MacConkey Agar Biplates (Lot 213926) for potential Listeria monocytogenes contamination, which may cause foodborne illness if used in diagnostics.
Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.
Remel is recalling 100 Blood Agar MacConkey Agar Biplates due to possible Listeria monocytogenes contamination. This could lead to foodborne illness if the contaminated plates are used in diagnostic testing.
The biplates may contain Listeria monocytogenes, a bacterium that can cause foodborne illness. Contamination is visible on the blood side of the biplate once removed from packaging, but the risk depends on proper handling during diagnostic use.
Users of these biplates for in vitro diagnostic testing are affected. Laboratory staff and healthcare professionals who handle the product are most at risk.
Check for the product name 'Blood Agar MacConkey Agar Biplate', reference number R02049, and lot number 213926. The expiration date is February 24, 2025.
Verify the product name, reference number R02049, and lot number 213926 to confirm if you have the recalled item.
The product may contain Listeria monocytogenes, which can cause foodborne illness if used in diagnostic testing. Proper handling is needed to minimize risk.
Look for the product name 'Blood Agar MacConkey Agar Biplate', reference number R02049, and lot number 213926. The expiration date is February 24, 2025.
The recall record does not specify a remedy, so contact Remel, Inc for guidance on handling the product.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-1200-2025 — Remel Remel Hello, I own a Remel that is covered by recall Z-1200-2025 from Remel. 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.
