Bethel Nutritional Consulting, Inc recalls SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
- Recall date
- December 19, 2014
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1207-2015
- FDA classification
- Class I
- Brand / firm
- Bethel Nutritional Consulting, Inc
- Sold / distributed
- Nationwide
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.
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
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