Abbott recalls ID NOW COVID-19 2.0 24T software with higher invalid rates. Affected lots may produce inaccurate test results. Consumers should check model and lot numbers for recall details.
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
Abbott is recalling ID NOW COVID-19 2.0 24T test devices with software version 192-000 that have a higher chance of giving invalid results. This could lead to inaccurate test outcomes, which is important for people relying on these tests for COVID-19 detection.
The recalled software versions have a higher occurrence of invalid rates compared to the product's instructions. This means the device might not work correctly, potentially leading to inaccurate test results for COVID-19 detection.
People who own the ID NOW COVID-19 2.0 24T test device with model number 192-000 and the listed lot numbers are affected. Those using the device for home testing are most at risk of inaccurate results.
Check your device's model number (192-000) and lot number (e.g., 000M884910, 000M913227, etc.) on the packaging or device itself. The product has a GTIN/DI of 10811877011351.
Identify your device's model number (192-000) and lot number from the packaging or device label.
The recall is due to higher occurrence of invalid rates compared to the product's instructions, which could lead to inaccurate test results.
Check your device's model number (192-000) and lot number (e.g., 000M884910, 000M913227) against the listed lots in the recall notice.
The recall does not require immediate action, but you should check your device's details to confirm if it's affected.
We’ve drafted a message you can send ID NOW to request your refund or repair — edit it as you like.
Subject: Recall Z-1571-2025 — ID NOW ID NOW Hello, I own a ID NOW that is covered by recall Z-1571-2025 from ID NOW. 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.
