Biomerieux recalls ETEST Clinical Eravacycline Erv US S30 (CATALOG 421553) due to temperature and time exposure risks affecting product performance. Affected units include specific batch numbers and UDI/DI codes.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling ETEST Clinical Eravacycline Erv US S30 products because they may not work properly if stored outside recommended temperature and time ranges. This could lead to inaccurate test results if used in clinical settings.
The product may not function correctly if stored outside the manufacturer's specified temperature and time ranges. This could result in inaccurate test results during clinical use.
Healthcare professionals using the ETEST Clinical Eravacycline Erv US S30 for clinical testing are most likely affected. The recall targets specific batch numbers and UDI/DI codes.
Check for the product name 'ETEST Clinical Eravacycline Erv US S30' with catalog number 421553. Affected units have UDI/DI code 03573026560997 and batch numbers starting with 1009288050.
Verify the product name, catalog number, UDI/DI code, and batch numbers to confirm if your item is affected.
The product may not work properly if stored outside the manufacturer's specified temperature and time ranges, which could lead to inaccurate test results.
Check for the product name 'ETEST Clinical Eravacycline Erv US S30' with catalog number 421553, UDI/DI code 03573026560997, and batch numbers starting with 1009288050.
The recall does not specify a remedy, so you should check product details to confirm if it's affected and contact Biomerieux for further guidance.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0851-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0851-2023 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.
