Biomerieux recalls BIOBALL B.SPIZENII NCTC 10400 550X20 (Catalog 56012) due to potential performance issues from temperature and time out of range. Affected units have 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 a specific bacterial culture product (BIOBALL B.SPIZIZENII NCTC 10400 550X20) because it may not perform correctly if stored outside recommended temperature and time ranges. This could affect lab results or testing accuracy.
The product may not function correctly if stored outside the manufacturer's specified temperature and time ranges. This could lead to inaccurate lab results or testing outcomes.
Lab users who own or use this specific bacterial culture product for testing. Those handling the product without proper temperature control are most at risk.
Check for the product name 'BIOBALL B.SPIZIZENII NCTC 10400 550X20' with catalog number 56012. Affected units have UDI/DI code 03573026228200 and batch numbers starting with 7190.
Verify the product name, catalog number, UDI/DI code, and batch numbers to confirm if your item is affected.
The product may not perform correctly if stored outside the manufacturer's specified temperature and time ranges, potentially affecting lab results.
The recall does not specify a remedy, so check the product details to confirm if it's affected and contact Biomerieux for further guidance.
Look for the product name 'BIOBALL B.SPIZIZENII NCTC 10400 550X20', catalog number 56012, UDI/DI code 03573026228200, and batch numbers starting with 7190.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0806-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0806-2023 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.
