SLIM-K — Class I drug recall D-1207-2015
Terminated recall by Bethel Nutritional Consulting, Inc, reported 2015-07-15, distributed nationwide. Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phen
| Recall number | D-1207-2015 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bethel Nutritional Consulting, Inc, New York, NY, United States |
| Recall initiated | 2014-12-19 |
| Classified | 2015-07-06 |
| Reported by FDA | 2015-07-15 |
| Terminated | 2018-06-27 |
| Distributed | Nationwide (US) |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00160126417509 |
| Lot numbers | 12/17, 140430 |
Product
SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
Reason for recall
Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.
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-1207-2015. 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.