Ameditech recalls First Check 1 Panel Drug Cup (AMT 990: All lots within expiry) due to inconsistent drug detection. Consumers should contact for remedy.
Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.
Ameditech recalls its First Check 1 Panel Drug Cup for inconsistent drug detection results. This could lead to inaccurate test outcomes if used without proper calibration.
The drug cup's immunoassay enzymes fail to consistently detect calibrators and secondary compounds as labeled. This means test results may be inaccurate, potentially leading to false negatives or positives.
People using this drug testing cup for home drug screening. Those who rely on consistent results for legal or medical purposes are most at risk.
Check for the product name 'First Check 1 Panel Drug Cup' and AMT item number 990400B. All lots within expiry date are affected.
Reach out to Ameditech for instructions on how to handle the recalled product.
The product may not consistently detect drugs as labeled, so it is not recommended for reliable testing.
Look for the product name 'First Check 1 Panel Drug Cup' and AMT item number 990400B; all lots within expiry are affected.
Contact Ameditech for instructions on handling the recalled product.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-3046-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3046-2020 from Ameditech. 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.
