FDA recalls Neptune's Fix Tianept: Contains unapproved drug tianeptine, no safe use in US. Stop using immediately.
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Neptune Resources recalls Tianeptine tablets sold as 'Neptune's Fix' because they contain tianeptine, a substance not approved by the FDA for any medical use in the US. This means the product is unsafe and should not be used.
Tianeptine is not approved by the FDA for any medical use in the United States. Using this product could cause serious health risks due to its unapproved status.
Anyone who owns or uses Neptune's Fix Tianeptine Tablets Extended Relief. People with medical conditions or those taking other medications are at higher risk.
Check for Neptune's Fix Tianeptine Tablets Extended Relief, 20 tablets per box, labeled 'Wide Awake, 3000 mg (150 mg per tablet)'. All lots are affected.
Immediately stop using Neptune's Fix Tianeptine Tablets Extended Relief as it contains an unapproved drug.
No, the FDA has determined that tianeptine is not approved for any medical use in the US, making this product unsafe.
Stop using it immediately and contact Neptune Resources for further instructions.
People with medical conditions or those taking other medications may be at higher risk due to the unapproved drug.
We’ve drafted a message you can send Neptune Resources to request your refund or repair — edit it as you like.
Subject: Recall D-0335-2024 — Neptune Resources Neptune Resources Hello, I own a Neptune Resources that is covered by recall D-0335-2024 from Neptune Resources. 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.