BioMerieux recalls VIDAS Measles IgG (MSG) test REF 30219 due to substrate errors causing potential delayed results. Affected units have specific UDI and lot numbers.
bioMerieux has been receiving an increasing number of complaints linked to a VIDAS substrate error. It prevents the test from being run, therefore leads to potential delayed results as the user must run another test.
BioMerieux is recalling VIDAS Measles IgG (MSG) tests with serial number 03573026064532 and lot number 1008890110 because a substrate error prevents the test from running, leading to potential delayed results. This means users may need to repeat the test, causing delays in diagnosis.
The test substrate has an error that prevents the test from running correctly. This means users must repeat the test, which can cause delays in getting results. The issue does not cause injury or damage to the user.
People who purchased or use the VIDAS Measles IgG (MSG) test with UDI 03573026064532 and lot number 1008890110 are affected. Those who need measles testing are most at risk of delayed results.
Check for the UDI number 03573026064532 and lot number 1008890110 on the test packaging. The product is labeled as VIDAS Measles IgG (MSG) with reference number 30219.
Look for the UDI number 03573026064532 and lot number 1008890110 on the test packaging.
BioMerieux has received complaints about a substrate error that prevents the test from running, leading to potential delayed results.
Check the test packaging for the UDI number 03573026064532 and lot number 1008890110. If it matches, you may need to repeat the test.
The recall does not provide a fix; users must repeat the test if the error occurs.
We’ve drafted a message you can send BioMerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0430-2022 — BioMerieux BioMerieux Hello, I own a BioMerieux that is covered by recall Z-0430-2022 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.
