SLIM-K recall
SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
Why was SLIM-K recalled?
Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # 140430; Exp.12/17
- Product
- SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.
- Recalling firm
- Bethel Nutritional Consulting, Inc
- Quantity
- UNKNOWN
- Distribution
- Nationwide
- Recall date
- July 15, 2015
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)