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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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Critical RiskFDA Drug
Medications & Supplements/Dietary Supplements

Neptune's Fix Tianeptine Elixirs and Tablets Recalled for Unapproved Drug

Agency Publication Date: February 16, 2024
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Summary

Neptune Resources, LLC is recalling 1,121,932 units of its Neptune's Fix products, including Tianeptine Elixir, Tianeptine Extra Strength Elixir, and Tianeptine Tablets Extended Relief. These products contain tianeptine, an unapproved substance that is not FDA-approved for any medical use in the United States and can be dangerous to consumers. The recall includes all lots of these products, which were distributed nationwide in bottles and boxes.

Risk

These products contain tianeptine, which is not approved for medical use and can lead to serious health issues. Consumers may experience severe adverse reactions including seizures, loss of consciousness, and potentially life-threatening incidents.

What You Should Do

  1. This recall affects all lots of Neptune's Fix Tianeptine Elixir (0.338 fl oz/10 mL), Neptune's Fix Tianeptine Extra Strength Elixir (0.338 fl oz/10 mL), and Neptune's Fix Tianeptine Tablets Extended Relief (20 tablets per box).
  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 Neptune Resources, LLC 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:

💰Option 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
🗑️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: Neptune's Fix Tianeptine Elixir, Fast Acting (0.338 fl oz / 10 mL)
Variants: 0.338 fl oz, 10 mL
Lot Numbers:
All lots

Distributed by Neptune Resources, LLC.

Product: Neptune's Fix Tianeptine Extra Strength Elixir (0.338 fl oz / 10 mL)
Variants: Extra Strength, 0.338 fl oz, 10 mL
Lot Numbers:
All lots

Distributed by Neptune Resources, LLC.

Product: Neptune's Fix Tianeptine Tablets Extended Relief (20 Tablets)
Variants: Tablets, Extended Relief, 3000 mg, 150 mg Per Tablet, Twenty Tablets per Box
Lot Numbers:
All lots

Distributed by Neptune Resources, LLC.

Product Images

Neptune's Fix Elixir

Neptune's Fix Elixir

Neptune's Fix Extra Strength Elixir

Neptune's Fix Extra Strength Elixir

Neptune's Fix Extra Strength Elixir Tablets

Neptune's Fix Extra Strength Elixir Tablets

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93808
Status: Active
Manufacturer: Neptune Resources, LLC
Sold By: Retailers nationwide
Manufactured In: United States
Units Affected: 3 products (1,000,000 bottles; 117,000 bottles; 4,932 boxes)
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 · FDA Press Release · 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.