Biomerieux recalls 60-measles IGG test kits (catalog 30219) due to temperature and time exposure risks. These tests may not work correctly if stored or used outside recommended conditions.
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Biomerieux is recalling 60-measles IGG test kits that may not work properly if exposed to temperatures or times outside the recommended range. This could lead to inaccurate test results if used incorrectly.
The test kits require specific temperature and time conditions to function correctly. If stored or used outside these conditions, the product may not provide accurate results, potentially leading to incorrect diagnoses.
People who purchased the Biomerieux Measles IGG 60-test kit (catalog 30219) for clinical use are likely affected. Healthcare workers and labs using these tests are at the highest risk.
Check for the product name 'VIDAS CLINICAL VIDAS MEASLES IGG 60TESTS' and catalog number 30219. The batch numbers listed are 1009421810.
Ensure the test kit is stored and used within the manufacturer's specified temperature and time range for accurate results.
No, but you should check if the test kit has been exposed to temperatures or times outside the recommended range.
The test may not provide accurate results, which could lead to incorrect diagnoses.
Look for the product name 'VIDAS CLINICAL VIDAS MEASLES IGG 60TESTS' and catalog number 30219 with batch number 1009421810.
We’ve drafted a message you can send Biomerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0796-2023 — Biomerieux Biomerieux Hello, I own a Biomerieux that is covered by recall Z-0796-2023 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.