SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
FDA Recall #D-1207-2015 — Class I — December 19, 2014
Product Description
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.
Recalling Firm
Bethel Nutritional Consulting, Inc — New York, NY
Classification
Class I — Reasonable probability of serious adverse health consequences or death.
Product Type
Drugs
Product Quantity
UNKNOWN
Distribution
Nationwide
Code Information
Lot # 140430; Exp.12/17
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated