Caffeine Powder — Class II drug recall D-1096-2017
Terminated recall by Global Marketing Enterprises, Inc., reported 2017-08-23, distributed in KY, MI, VA. Marketed without an Approved NDA/ANDA: The product consists of pure, powdered caffeine and is an unapproved dr
| Recall number | D-1096-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Global Marketing Enterprises, Inc., Chicago, IL, United States |
| Recall initiated | 2017-05-22 |
| Classified | 2017-08-17 |
| Reported by FDA | 2017-08-23 |
| Terminated | 2022-08-25 |
| Distributed | KY, MI, VA |
| Quantity | 52.5 kilograms |
| Reason classes | labeling, unapproved product |
| UPC / GTIN / UDI-DI | 00021754905076 |
| Lot numbers | 12/19, 15121931, 15121939 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1096-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.