Remel recalls Blood/MacConkey Biplate 100/PK (Product R02049) due to potential Listeria monocytogenes contamination. Affected units include specific lot numbers and UDI-DI codes. Consumers should check their product details and take action if applicable.
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Remel is recalling Blood/MacConkey Biplate 100/PK products that may contain Listeria monocytogenes, a bacteria that can cause serious illness. This recall is important because Listeria contamination in lab culture media could lead to foodborne illness if used improperly.
Listeria monocytogenes is a bacterium that can cause serious infections, especially in pregnant women, newborns, and immunocompromised individuals. Contamination in lab culture media could lead to the bacteria being introduced into samples or environments where it might spread to people.
Laboratory users and researchers who own or use the Blood/MacConkey Biplate 100/PK products with the specified lot numbers and UDI-DI code. Those handling the products in a lab setting are most at risk.
Check for the product number R02049, lot number 274194, and UDI-DI code 848838003684 on the packaging. The recall applies to specific batches sold by Remel, Inc.
Verify your Blood/MacConkey Biplate 100/PK has the product number R02049, lot number 274194, and UDI-DI code 848838003684.
The recall states the products may contain Listeria monocytogenes, but it does not specify if the product is safe to use. Consumers should check their specific product details and follow the recall instructions.
The recall does not provide a remedy, so there is no specific action required beyond checking if your product matches the recall details.
Check for the product number R02049, lot number 274194, and UDI-DI code 848838003684 on the packaging. If your product matches these details, it is affected.
We’ve drafted a message you can send Remel to request your refund or repair — edit it as you like.
Subject: Recall Z-2226-2025 — Remel Remel Hello, I own a Remel that is covered by recall Z-2226-2025 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.
