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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Over-the-Counter

Neuroquell and Neuroquell Plus Recalled for cGMP Violations

Agency Publication Date: September 10, 2025
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Summary

Atlantic Management Resources Ltd. is recalling 72 containers of Neuroquell and Neuroquell Plus (.22 fl. oz) due to violations of current Good Manufacturing Practice (cGMP) regulations. These violations suggest the products may not have been manufactured under adequate safety and quality controls. The affected products were distributed exclusively via the internet.

Risk

Failure to follow Good Manufacturing Practices can result in products that are contaminated, have incorrect potencies, or lack the quality standards necessary to ensure consumer safety. There are no reported injuries at this time.

What You Should Do

  1. Check your product packaging for Neuroquell or Neuroquell Plus (.22 fl. oz) with NDC 66233712-01 and lot numbers B-02, 1087920520, or 1087920920.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Atlantic Management Resources Ltd. for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Neuroquell & Neuroquell Plus (0.22 fl. oz / 6.6mL)
Model:
R937
Lot Numbers:
B-02
1087920520 (BBE 05/31/21)
1087920920 (BBE 05/31/21)
NDC:
66233712-01

Mfg. For/Dist. By Claire Ellen Products, P.O. Box 901 Westboro, MA 01581 USA

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97345
Status: Active
Manufacturer: Atlantic Management Resources Ltd.
Sold By: Internet
Manufactured In: United States
Units Affected: 72 containers
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.