Ameditech recalls First Check 4 Panel Drug Cups due to inconsistent detection of calibrators and compounds, potentially leading to inaccurate drug test results.
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 is recalling its First Check 4 Panel Drug Cups because they may not consistently detect drugs in samples as labeled. This could lead to inaccurate test results, which is important for users relying on these tests.
The drug cups may not consistently detect all calibrators and compounds at the levels stated on the label. This means test results could be inaccurate, potentially leading to false negatives or positives.
Users of the First Check 4 Panel Drug Cups who are testing for drugs may be affected. Those who rely on accurate drug test results are at higher risk.
Check for the product name 'First Check 4 Panel Drug Cup' with AMT Item Number 990100B. All lots within the expiry date are affected.
Verify the product name and AMT Item Number 990100B to confirm if your cup is recalled.
The drug cups may not consistently detect all calibrators and compounds at the levels stated in the labeling, potentially causing inaccurate test results.
Check the product name and AMT Item Number 990100B to confirm if it's recalled; no specific action is required beyond verification.
The recall record does not mention any remedy or fix for this product.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-3049-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3049-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
