Neptune's Fix — Class I drug recall D-0393-2024
Terminated recall by Super Chill Products, reported 2024-03-27, distributed nationwide. Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medic
| Recall number | D-0393-2024 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Super Chill Products, New York, NY, United States |
| Recall initiated | 2024-02-05 |
| Classified | 2024-03-21 |
| Reported by FDA | 2024-03-27 |
| Terminated | 2024-08-20 |
| Distributed | Nationwide (US) |
| Quantity | 3,573 bottles |
| Reason classes | unapproved product |
Product
Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.
Reason for recall
Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0393-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.