Ameditech recalls QuickTox Drug Screen DipCards QT70, QT88, QT11, QT52, QT44, QT23, QT80F, QT52A, and QT20 due to inconsistent drug detection results from enzyme failures in immunoassay.
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 several QuickTox Drug Screen DipCards because they may not consistently detect drugs as labeled due to enzyme failures. This means users could get inaccurate results, which is risky for drug testing accuracy.
The dipcards use immunoassay enzymes that have failed to work properly, causing inconsistent detection of drugs. This means the products might not detect all drugs at the levels stated on the label, leading to inaccurate test results.
People who own or use QuickTox Drug Screen DipCards QT70, QT88, QT11, QT52, QT44, QT23, QT80F, QT52A, or QT20 for drug testing are affected. Those testing for drugs without reliable results are most at risk.
Check for QuickTox Drug Screen DipCards with model numbers QT70, QT88, QT11, QT52, QT44, QT23, QT80F, QT52A, or QT20. These were sold with the same drug detection capabilities as listed in the product description.
Identify your QuickTox Drug Screen DipCard model number from the product description.
Ensure the test results match the expected drug detection levels listed on the product label.
The recall is due to immunoassay enzymes failing to consistently detect drugs, which could lead to inaccurate test results.
Models QT70, QT88, QT11, QT52, QT44, QT23, QT80F, QT52A, and QT20 are affected.
No, but you should verify test results match the expected detection levels to ensure accuracy.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-3043-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3043-2020 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.
