Ameditech recalls TDDA Drugs of Abuse Cups due to inconsistent drug detection. Products may not reliably identify all calibrators and compounds as labeled.
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 TDDA Drugs of Abuse Cups because they don't consistently detect all drugs as labeled. This could lead to inaccurate drug testing results.
The cups use immunoassay enzymes that fail to perform consistently. This means they might not detect all calibrators and compounds at the levels specified on the label, leading to inaccurate test results.
Users of these drug testing cups, particularly those relying on them for accurate drug screening, are affected. The risk is low as the issue is with detection accuracy, not physical safety.
Look for the TDDA Drugs of Abuse Cup with model TDDA-6MBAU-CUP. All lots within expiry date are affected.
Identify the model number TDDA-6MBAU-CUP on the cup to confirm it is affected.
The cups may not consistently detect all drugs as labeled due to failed immunoassay enzymes.
The recall does not specify a remedy, so check the product details to confirm if it is affected.
The recall addresses inaccurate drug detection, not physical safety risks.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-3044-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3044-2020 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.
