Magic Slim capsules — Class I drug recall D-1379-2014
Terminated recall by MyNicNaxs, Inc., reported 2014-06-18, distributed nationwide. Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredien
| Recall number | D-1379-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MyNicNaxs, Inc., Deltona, FL, United States |
| Recall initiated | 2014-01-24 |
| Classified | 2014-06-12 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2019-10-02 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen, unapproved product |
Product
Magic Slim capsules, supplied in 60 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL
Reason for recall
Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredients: N-desmethylsibutramine, benzylsibutramine, and sibutramine
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-1379-2014. 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.