Biomerieux recalls PPM LOMBARD CT&TI-TSA products due to temperature and time out of range causing unreliable performance. Affected units include specific catalog and batch numbers.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling certain PPM LOMBARD products because they may not work properly if exposed to temperatures or times outside the safe range. This could lead to unreliable results in testing.
The products may not function correctly if stored or used outside the specified temperature and time ranges. This could lead to unreliable test results, but does not pose a direct safety risk like injury or fire.
Users of the PPM LOMB:CT&TI-TSA products with catalog number C6045-TI and batch numbers starting with 1009389930 are affected. Laboratory or clinical users who rely on these products for testing are most at risk.
Check for the catalog number C6045-TI and batch numbers starting with 1009389930 on the product label. The product is sold under the brand name PPM LOMBARD.
Look for catalog number C6045-TI and batch numbers starting with 1009389930 on the product label.
The PPM LOMBARD CT&TI-TSA + L & P80 10PLT products with catalog number C6045-TI and batch numbers starting with 1009389930.
The products may not work properly if exposed to temperatures or times outside the safe range, leading to unreliable test results.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0872-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0872-2023 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.
