Nuclein recalls DASH SARS-CoV-2 & Flu A/B Test Model SG-0006 due to potential false negatives. This may cause missed diagnosis or delayed treatment. Affected units have specific lot codes and expiration dates.
Due to manufacturing error, assay test may result in missed diagnosis or delay of treatment. (Potential false negative result)
Nuclein is recalling its DASH SARS-CoV-2 & Flu A/B Test Model SG-0006 because a manufacturing error might cause false negative results, meaning infections could go undetected or treatment delayed. This is serious for people relying on the test for accurate health monitoring.
The test may produce false negative results due to a manufacturing error, meaning infections could be missed or treatment delayed. This happens because the test might not detect the virus correctly when used properly.
People who own or use the DASH SARS-CoV-2 & Flu A/B Test Model SG-0006 (lot codes BB02 or BB03) are affected. Those who rely on this test for accurate diagnosis are most at risk.
Check for lot codes BB02 or BB03 on the test kit. The expiration date is February 20, 2026 for both lots. Each kit contains 10 tests.
Look for lot codes BB02 or BB03 on the test kit label.
Reach out to Nuclein LLC for further assistance if you have the affected lot codes.
Due to a manufacturing error, the test may result in missed diagnosis or delayed treatment by producing false negative results.
Check the lot code on your test kit. If it's BB02 or BB03, contact Nuclein LLC for guidance.
No, the hazard is a potential false negative result, which could lead to missed diagnosis or delayed treatment, but it does not cause physical injury.
We’ve drafted a message you can send Nuclein to request your refund or repair — edit it as you like.
Subject: Recall Z-2274-2025 — Nuclein Nuclein Hello, I own a Nuclein that is covered by recall Z-2274-2025 from Nuclein. 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.
