D-1207-2015 Class I Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- July 15, 2015
- Initiation Date
- December 19, 2014
- Termination Date
- June 27, 2018
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- UNKNOWN
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.
Distribution Pattern
Nationwide
Code Information
Lot # 140430; Exp.12/17