SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.
What was recalled
SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
- Recalling firm
- Bethel Nutritional Consulting, Inc
- Origin
- NY, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1207-2015
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
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