bioMerieux recalls VIDAS PRG Progesterone tests with specific lot numbers due to substrate errors causing potential test delays. Affected users should contact for details.
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 certain VIDAS PRG Progesterone tests because of a substrate error that prevents the test from running, leading to potential delayed results. This means users may need to repeat the test, which could cause delays in getting results.
The substrate error prevents the test from running correctly, requiring users to repeat the test. This can lead to delayed results, which might affect medical decisions if the test is time-sensitive.
Users of the VIDAS PRG Progesterone test with specific lot numbers are affected. Those who rely on timely test results for medical decisions are at higher risk.
Check the lot numbers on the test: 1008685490, 1008766980, 1008775630, 1008873180, 1008911240. The product is labeled as VIDAS PRG Progesterone, REF 30409-01.
Look for the lot numbers 1008685490, 1008766980, 1008775630, 1008873180, or 1008911240 on the test.
bioMerieux has received complaints about a substrate error that prevents the test from running, leading to potential delayed results.
Check the lot number on the test. If it matches the listed numbers, contact bioMerieux for further instructions.
Yes, but you may need to repeat the test if the substrate error occurs, which could delay results.
We’ve drafted a message you can send bioMerieux to request your refund or repair — edit it as you like.
Subject: Recall Z-0424-2022 — bioMerieux bioMerieux Hello, I own a bioMerieux that is covered by recall Z-0424-2022 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.
