Abbott recalls ID NOW Influen: 427-000 kit with higher invalid rates than normal use. Consumers should check lot numbers on packaging.
It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.
Abbott is recalling its ID NOW Influenza A & B 2 test kit (model 427-000) because some batches produce more invalid results than expected. This could lead to inaccurate test outcomes if used.
The test kit has a higher rate of invalid results in some batches. This means the test might not work properly, leading to inaccurate flu detection. The issue is not a safety hazard but affects test reliability.
People who purchased or use the ID NOW Influenza A & B 2 test kit (model 427-000) between 2022 and 2027. Those most at risk are users who rely on this test for frequent flu screening.
Check the model number on the packaging: 427-000. The lot number starts with 000X133126 and expires by February 21, 2027.
Look for the lot number on the packaging, which starts with 000X133126.
No, the recall is for potential inaccurate results, not a safety hazard.
Check the model number on the packaging: 427-000. The lot number starts with 000X133126 and expires by February 21, 2027.
The recall does not require immediate action. Check the lot number and contact Abbott if you have concerns.
We’ve drafted a message you can send Abbott to request your refund or repair — edit it as you like.
Subject: Recall Z-1565-2026 — Abbott Abbott Hello, I own a Abbott that is covered by recall Z-1565-2026 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.
