Biomerieux recalls API Listeria 10 Strips+10 Media (Catalog 10300) due to potential performance issues from temperature and time exposure. Affected units have specific batch and UDI/DI numbers.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling API Listeria 10 Strips+10 Media (Catalog 10300) because the product may not perform correctly if stored outside recommended temperature and time ranges. This could affect lab results if used improperly.
The product may not function correctly if stored outside the manufacturer's specified temperature and time ranges. This could lead to inaccurate lab results if the product is used without proper conditions.
Laboratory users who own or use the API Listeria 10 Strips+10 Media (Catalog 10300) with UDI/DI 03573026035587 and batch number 1009418280 are affected. Lab technicians and researchers using this product are most at risk.
Check for the product name 'API Listeria 10 Strips+10 Media', catalog number 10300, UDI/DI 03573026035587, and batch number 1009418280 on the packaging.
Verify the product name, catalog number, UDI/DI, and batch number on the packaging to confirm if it's affected.
The recall states the product may not perform correctly if temperature and time conditions are exceeded, but it does not indicate immediate danger if used properly.
The recall record does not specify a remedy, so no action is required beyond checking the product details.
Check for the product name 'API Listeria 10 Strips+10 Media', catalog number 10300, UDI/DI 03573026035587, and batch number 1009418280 on the packaging.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0783-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0783-2023 from Biomerieux. 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.
