Ameditech recalls First Check 2 Panel Drug Cup (THC/COC) due to inconsistent detection of drugs. All lots within expiry are affected. 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 all First Check 2 Panel Drug Cups (THC/COC) because they may not consistently detect drugs as labeled. This could lead to inaccurate test results if used for drug screening.
The drug testing cup uses enzymes that sometimes fail to work properly. This means it might not detect all drugs at the levels claimed on the label, leading to false negatives or false positives.
People who use this drug testing cup for home drug screening. Those testing for THC or cocaine may be at risk of inaccurate results.
Check for the product name 'First Check 2 Panel Drug Cup' with AMT Item Number 990600B. All lots within expiry dates 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 2 Panel Drug Cup' with AMT Item Number 990600B. All lots within expiry are affected.
Contact Ameditech for instructions on how to handle 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-3048-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3048-2020 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.
