Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Caffeine Powder Recalled by Global Marketing Enterprises, Inc. Due to Marketed without an Approved NDA/ANDA: The product consists...

Date: May 22, 2017
Company: Global Marketing Enterprises, 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 Global Marketing Enterprises, Inc. directly.

Affected Products

Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz)., 1250 servings, Packed By: LifeLine Nutrients Corp, 1801 S. Canal St, Chicago, IL 60616, UPC 021754905076

Quantity: 52.5 kg

Why Was This Recalled?

Marketed without an Approved NDA/ANDA: The product consists of pure, powdered caffeine and is an unapproved drug due to stimulant claims. The product is also misbranded as it fails to bear adequate directions for its intended use.

Where Was This Sold?

This product was distributed to 3 states: KY, MI, VA

Affected (3 states)Not affected

About Global Marketing Enterprises, Inc.

Global Marketing Enterprises, Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

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