Ameditech recalls drug screening sheets that may not consistently detect drugs due to enzyme failures. Affected products include specific lot numbers and catalog codes.
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 certain drug screening sheets that may not consistently detect drugs because of enzyme failures. This could lead to inaccurate results in drug testing. Users should check if their sheets match the listed product codes and lots.
The drug screening sheets contain enzymes that failed to work properly, causing inconsistent detection of drugs. This means the tests might not detect all drugs at the levels stated on the label, leading to false negatives.
People who own or use these drug screening sheets for testing are affected. Those testing for drugs in a medical or legal context are most at risk of inaccurate results.
Check for the product codes and lot numbers listed in the recall: EDI OPI (300) Uncut Sheet-Card (lot 100163), EDI PPX Uncut Sheet-Card (lot 187876), and other specific sheet types with their corresponding lot numbers. Also, check if the product includes catalog numbers like 31105-3 or lot numbers from the updated list.
Look for the product codes and lot numbers listed in the recall to confirm if your sheets are affected.
No, the recall states the sheets may not consistently detect drugs but does not mention physical injury risks.
Check for the specific product codes and lot numbers listed in the recall, such as EDI OPI (300) Uncut Sheet-Card (lot 100163) or EDI PPX Uncut Sheet-Card (lot 187876).
The recall does not specify a remedy, so you should check the product details to confirm if they are affected and contact Ameditech for further guidance.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-3051-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3051-2020 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.
