Ameditech recalls ImmuTest Drugs of Abuse Cups due to inconsistent drug detection results. Products may fail to detect all calibrators and compounds as labeled, risking inaccurate test outcomes.
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 ImmuTest Drugs of Abuse Cups because they don't consistently detect all drugs as labeled. This could lead to false negative results, meaning some drug use might go undetected.
The cups use immunoassay enzymes that sometimes fail to work properly. This means the test might not detect all drugs at the levels stated on the label, leading to false negatives where drug use goes undetected.
People who use these drug testing cups for workplace or legal compliance testing. Those testing for specific drugs like cocaine, THC, or opioids may be at higher risk of inaccurate results.
Check for model numbers IMCA-5AB-W, IMC-8BBCE, or IMCA-8CM5 on the cup. These cups were sold with specific drug detection capabilities and are part of the recall.
Look for model numbers IMCA-5AB-W, IMC-8BBCE, or IMCA-8CM5 on the cup.
The product may not consistently detect all drugs as labeled due to failed immunoassay enzymes.
Check the model number to see if it's in the recall list. If it is, stop using it and contact Ameditech for further instructions.
The product does not pose a safety risk but may give false negative results, meaning drug use could go undetected.
We’ve drafted a message you can send Ameditech to request your refund or repair — edit it as you like.
Subject: Recall Z-3036-2020 — Ameditech Ameditech Hello, I own a Ameditech that is covered by recall Z-3036-2020 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.
