FDA Drug recall D-1207-2015
SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc
- FDA Drug
- Class I
- terminated
- Published 2015-07-15
On 2015-07-15 the FDA classified a Class I recall of SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc by Bethel Nutritional Consulting, citing marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1207-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2014-12-19 |
| Published | 2015-07-15 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Bethel Nutritional Consulting |
| Distribution | US |
Product
SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
Reason
Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.
Identifiers
| code_info | Lot # 140430; Exp.12/17 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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FDA Drug · Class I · 2013-12-25 · Bethel Nutritional Consulting - Bethel 30 capsules, packaged in 30 count bottles, Distributed by BETHEL INC. New York, New York
FDA Drug · Class I · 2013-09-04 · Bethel Nutritional Consulting
All Bethel Nutritional Consulting recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1207-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.