Biomerieux recalls ETEST Amoxi/Clav 2/1 XL 256 US S30 due to temperature and time issues affecting product performance. No remedy specified in official notice.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling its ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30 test kits because they may not work properly if stored or used outside the correct temperature and time range. This could lead to inaccurate test results if the product is not handled correctly.
The test kits may not function correctly if stored or used outside the required temperature and time range. This could result in inaccurate test results, which might affect medical decisions.
Healthcare professionals and labs using the ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30 test kits are most at risk if they rely on the product for accurate results. The recall affects specific batch numbers and model numbers.
Check for the model number ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, catalog number 412252, and batch numbers starting with 1009311920. The product was sold with a specific UDI/DI code 03573026376703.
Identify the model number, catalog number, and batch numbers to confirm if your product is affected.
The product may not work correctly if stored or used outside the required temperature and time range, which could lead to inaccurate test results.
The official recall notice does not specify a remedy, so you should check the product details to confirm if it is affected.
Look for the model number ETEST CLINICAL AMOXI/CLAV 2/1 XL 256 US S30, catalog number 412252, and batch numbers starting with 1009311920.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0819-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0819-2023 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.
