Biomerieux recalls ETEST Clinical Imipenem Relebactam IPR US S30 due to potential performance issues from temperature and time out of range. Affected units include 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 Imipenem Relebactam IPR US S30 products because they may not perform correctly if exposed to temperatures or times outside the specified range. This could affect the reliability of the product in clinical settings.
The product may not function properly if stored or used outside the recommended temperature and time ranges. This could lead to unreliable test results in clinical environments.
Healthcare professionals using the ETEST Clinical Imipenem Relebactam IPR US S30 product are most likely affected. The risk is low as the issue relates to product performance rather than immediate safety hazards.
Check for the product name 'ETEST Clinical Imipenem Relebactam IPR US S30' and catalog number 420927. Affected units include batch numbers starting with 1008988170.
Verify the product name, catalog number, and batch numbers to confirm if your item is affected.
The product may not perform correctly if exposed to temperatures or times outside the specified range, but it does not pose an immediate safety risk.
The recall does not specify a remedy, so check the product details to confirm if it is affected and contact Biomerieux for further guidance.
Look for the product name 'ETEST Clinical Imipenem Relebactam IPR US S30' and catalog number 420927. Affected units include batch numbers starting with 1008988170.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0849-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0849-2023 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.
