Biomerieux recalls API 20 E 2:25 Strips (Catalog 20100) due to potential performance issues from temperature and time exposure. Affected units may not function correctly.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling API 20 E 25 Strips (Catalog 20100) because they might not work properly if stored outside recommended temperature and time ranges. This could affect test results in medical labs.
The strips may not perform correctly if stored outside the manufacturer's specified temperature and time ranges. This could lead to inaccurate test results in medical settings.
Medical labs and healthcare professionals using these test strips. Those who rely on accurate test results are most at risk.
Look for the product name 'API 20 E 25 STRIPS' with catalog number 20100. Check the batch number on the packaging, which starts with 1009226560.
Verify the catalog number (20100) and batch number (1009226560) on the packaging.
The product may not function correctly if stored outside the manufacturer's specified temperature and time ranges.
The recall does not specify a remedy, so no action is required beyond checking product details.
The recall does not mention any injury risk, only potential performance issues.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0784-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0784-2023 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.