Biomerieux recalls PPM Industry Combourg Chromid Carba US 20 PL: Product may not function correctly if temperature or time outside specified range.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling a specific type of laboratory test kit because it may not work properly if kept at temperatures or for durations outside the manufacturer's specified range. This could lead to inaccurate test results.
The product may not function correctly if the temperature or time outside the specified range is exceeded. This could result in inaccurate test results, especially in laboratory settings where precision is critical.
Laboratory users who purchased the PPM Industry Combourg Chromid Carba US 20 PLT test kit with catalog number 414012 and batch number 2147080 are affected. Those using the product for critical testing may be at higher risk.
Check for the catalog number 414012 and batch number 2147080 on the product label. The product was sold with a unique identifier (UDI/DI) 03573026409913.
Verify the catalog number 414012 and batch number 2147080 on the product label.
The product may not function correctly if temperature or time outside the specified range is exceeded, but it does not pose a direct safety risk like injury or fire.
The recall does not specify a remedy, so no action is required beyond checking the product details.
Look for the catalog number 414012 and batch number 2147080 on the product label, or the unique identifier 03573026409913.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0839-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0839-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
