Biomerieux recalls ETEST Clinical Benzylpenicillin PG 256 US S30 (Catalog 412262) due to potential performance issues from temperature and time out of range. Affected units include specific batch numbers.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling a specific type of benzylpenicillin test kit because it 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 recommended temperature and time range. This could result in inaccurate test results, but does not pose an immediate physical danger to users.
Healthcare professionals and labs using the ETEST Clinical Benzylpenicillin PG 256 US S30 test kits with batch numbers starting 1009477980 are most at risk. The recall affects specific laboratory equipment.
Check for the product name 'ETEST Clinical Benzylpenicillin PG 256 US S30' and catalog number 412262. Affected units have batch numbers starting with 1009477980.
Verify the product name, catalog number, and batch number to confirm if it is affected.
No immediate physical danger, but the test kits may not work correctly if stored outside the recommended temperature and time range.
Check the product details to confirm if it is affected; no specific action is required if it is not in the recalled batch range.
Look for the product name 'ETEST Clinical Benzylpenicillin PG 256 US S30' and catalog number 412262 with batch numbers starting with 1009477980.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0820-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0820-2023 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.
