Biomerieux recalls ETEST CEFTOLOZANE/TAZOL C/T US S30 due to temperature and time issues affecting product performance. Affected units have catalog number 414445 and batch numbers starting with 1009420460.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling ETEST CEFTOLOZANE/TAZO C/T US S30 test kits because they may not work properly if stored outside the recommended temperature and time range. This could lead to inaccurate test results if used incorrectly.
The test kits may not function correctly if stored outside the specified temperature and time range. This could result in inaccurate test results, but does not pose a direct risk of injury or harm to users.
Users of the ETEST CEFTOLOZANE/TAZO C/T US S30 test kits, particularly those in clinical labs or healthcare settings that rely on these tests. The risk is low for most users as the issue relates to storage conditions rather than immediate safety hazards.
Check for the catalog number 414445 and batch numbers starting with 1009420460 on the product label. The product is sold by Biomerieux Inc and used in clinical testing environments.
Look for the catalog number 414445 and batch numbers starting with 1009420460 on the product label.
The product may not work properly if stored outside the recommended temperature and time range, which could lead to inaccurate test results.
Check the product label for the catalog number 414445 and batch numbers starting with 1009420460. If you have the product, you may need to verify storage conditions to ensure proper performance.
No, the recall is for potential inaccurate test results due to storage conditions, not a direct safety hazard.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0841-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0841-2023 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.
