Ameditech recalls ProScreen drug test kits due to inconsistent detection of calibrators and compounds. Products may not reliably identify drugs as labeled. Consumers should check model numbers and lot dates for affected items.
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 ProScreen drug test kits because they may not consistently detect all drugs as stated on the label. This could lead to inaccurate results, especially for certain substances like cocaine and THC.
The test kits use enzymes that can fail to work properly, causing inconsistent detection of calibrators and secondary compounds. This means the products might not identify drugs at the levels specified on the label, leading to inaccurate results.
People who purchased ProScreen drug test kits from Ameditech. Those using the kits for workplace testing or personal use may be affected if they rely on the results.
Check the product model numbers like PSD-6MB, PSD-6MTDBO-300, or PSCUP-5M-W. The recall includes all lots within the expiry date as listed in the product descriptions.
Identify the specific model number from the product label, such as PSD-6MB or PSCUP-5M-W.
Ensure the product was manufactured within the expiry date listed in the recall notice.
The recall does not mention any injury risk; the issue is with test accuracy, not physical harm.
Check the model number on the product label, such as PSD-6MB, PSD-6MTDBO-300, or PSCUP-5M-W. The recall includes all lots within the expiry date.
The recall does not specify a remedy, so you may continue using the kit if you don't rely on the results for critical decisions.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-3042-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3042-2020 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.
