Slim Xtreme Weight loss capsules — Class I drug recall D-1378-2014
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-1378-2014 |
|---|---|
| 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
Slim Xtreme Weight loss capsules, 500 mg, supplied in 30 count bottles, Another product from Globe All Wellness, LLC Hollywood, FL 33020, distributed by MyNicKnaxs, LLC Deltona, FL
Reason for recall
Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredient: 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-1378-2014. 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.