Class I โ€” Serious Health Hazard

Serious health hazard โ€” there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.

SLIM-K Recalled by Bethel Nutritional Consulting, Inc Due to Marketed Without An Approved NDA/ANDA: Product was found...

Date: December 19, 2014
Company: Bethel Nutritional Consulting, Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Bethel Nutritional Consulting, Inc directly.

Affected Products

SLIM-K, 30 Capsules, barcode 160126417509, Distributed by: Bethel Inc.

Quantity: UNKNOWN

Why Was This Recalled?

Marketed Without An Approved NDA/ANDA: Product was found to contain sibutramine, desmethylsibutramine and phenolphthalein based on FDA sampling and analysis.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Bethel Nutritional Consulting, Inc

Bethel Nutritional Consulting, Inc has 5 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report