# FDA recall D-1096-2017

> **Global Marketing Enterprises, Inc.** · Class II · drug recall initiated 2017-05-22.

## Product

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

## Reason for recall

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.

## Distribution

KY, VA, MI

## Key facts

- **Recall number:** D-1096-2017
- **Recalling firm:** Global Marketing Enterprises, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-05-22
- **Report date:** 2017-08-23
- **Termination date:** 2022-08-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chicago, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1096-2017

## Citation

> AI Analytics. FDA recall D-1096-2017. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1096-2017. Source: US FDA. Licensed CC0.

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