BLACK GOLD X ADVANCED capsules — Class I drug recall D-0221-2017
Terminated recall by Making It a Lifestyle, reported 2016-12-28, distributed nationwide. Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.
| Recall number | D-0221-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Making It a Lifestyle, Corpus Christi, TX, United States |
| Recall initiated | 2016-04-29 |
| Classified | 2016-12-22 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2020-09-30 |
| Distributed | Nationwide (US) |
| Quantity | 1,000 bottles |
| Reason classes | undeclared allergen, unapproved product |
Product
BLACK GOLD X ADVANCED capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.
Reason for recall
Marketed without an approved NDA/ANDA - presence of undeclared 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-0221-2017. 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.