Atlantic Management Resources Ltd. recalls Neuroquell and Neuroquell Plus due to cGMP violations. Products sold in the US with NDC 66233712-01 and specific batch numbers may be unsafe.
cGMP violations
Atlantic Management Resources Ltd. is recalling Neuroquell and Neuroquell Plus products because they were made under cGMP (current Good Manufacturing Practice) violations. This means the products may not be safe for use as intended.
cGMP violations mean the products were not made under the strict quality standards required for safe medication. This could lead to unsafe levels of active ingredients or contaminants in the product.
People who purchased Neuroquell or Neuroquell Plus from US retailers between May 2021 and the recall date are affected. Those who have the specific batch numbers listed are at higher risk.
Check the product label for the NDC code 66233712-01 and batch numbers 1087920520 or 1087920920. Products were sold in the US by Claire Ellen Products starting May 31, 2021.
Look for the NDC code 66233712-01 and batch numbers 1087920520 or 1087920920 on the product label.
The product was made under cGMP violations, which means it may not meet the safety standards required for medication.
Check the product label for the NDC code 66233712-01 and batch numbers 1087920520 or 1087920920. If you have these, stop using it and contact the manufacturer.
The recall notice does not specify a return deadline.
We’ve drafted a message you can send Atlantic Management Resources Ltd. to request your refund or repair — edit it as you like.
Subject: Recall D-0629-2025 — Atlantic Management Resources Ltd. Atlantic Management Resources Ltd. Hello, I own a Atlantic Management Resources Ltd. that is covered by recall D-0629-2025 from Atlantic Management Resources Ltd.. 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.