Abbott recalls ID NOW Influenza A/B 2 24T software with higher invalid rates than specified. Affected lots may produce inaccurate test results. Consumers should check model and lot numbers.
the impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
Abbott is recalling certain versions of its ID NOW Influenza A/B 2 24T test software due to higher rates of invalid test results compared to expected. This could lead to inaccurate influenza testing outcomes if the software is used.
The recalled software versions have a higher occurrence of invalid test results than the product's instructions specify. This means the test may not work properly, leading to inaccurate results for influenza A and B detection.
Users of the ID NOW Influenza A/B 2 24T test software with the specific model and lot numbers listed in the recall. Healthcare providers and labs using this software are most at risk of inaccurate test results.
Check for the model number 427-000 and lot numbers listed in the recall (e.g., 000M889669, 000M890889, etc.). The product is sold under the brand ID NOW Influenza A/B 2 24T.
Look for the lot number on the software packaging or label, which should match one of the listed lots (e.g., 000M889669, 000M890889).
The recalled software versions have a higher occurrence of invalid test results than the product's instructions specify, which could lead to inaccurate influenza testing.
Check the model number (427-000) and lot number on the software packaging; affected lots include 000M889669, 000M890889, and others listed in the recall.
The recall does not specify a remedy, so affected users should check the software's lot number and contact Abbott for further guidance.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1575-2025 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1575-2025 from Abbott. 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.
