Biomerieux recalls ETEST Meropenem MP 32 US S30 due to potential performance issues from temperature and time exposure. Affected units have specific batch numbers and catalog codes.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling ETEST CLINICAL MEROPENEM MP 32 US S30 test kits because they may not work properly if exposed to temperatures outside the recommended range. This could lead to inaccurate test results, which is important for medical diagnosis.
The test kits may not function correctly if stored or used outside the specified temperature and time limits. This can cause inaccurate results, potentially affecting medical decisions about antibiotic treatment.
Healthcare professionals and labs using the ETEST Meropenem MP 32 US S30 test kits with batch numbers 03573026378165 are affected. Those handling the product without proper temperature control are at higher risk of inaccurate results.
Check for the catalog number 412401 and batch number 03573026378165 on the product label. The product is sold under the ETEST CLINICAL MEROPENEM MP 32 US S30 name.
Look for the catalog number 412401 and batch number 03573026378165 on the product label.
The product may not work properly if exposed to temperatures outside the recommended range, which could lead to inaccurate test results.
Check the product label for the catalog number 412401 and batch number 03573026378165. If it matches, contact Biomerieux for guidance.
No serious injury risk is mentioned in the recall. The hazard is limited to potential inaccurate test results.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0827-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0827-2023 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.
