Global Marketing Enterprises, Inc. recalls Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz)., 1250 servings, Packed By:
Global Marketing Enterprises recalls unapproved caffeine powder due to lack of FDA approval and inadequate labeling. Consumers should check product details and contact the company for guidance.
Recall notice
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.
Contact the company & request your remedy
What happened, in plain English
Global Marketing Enterprises is recalling caffeine powder because it's marketed as a drug without FDA approval and lacks proper usage instructions. This poses a risk of improper use since it's not approved for human consumption. Read more at govinfonow.com/recall/41602-global-marketing-enterprises-caffeine-powder-recall-unapproved-drug-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/41602-global-marketing-enterprises-caffeine-powder-recall-unapproved-drug-risk · Updated October 8, 2026 · FDA enforcement record: FDA #D-1096-2017
Cite this page
“Global Marketing Enterprises Caffeine Powder Recall: Unapproved Drug Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/41602-global-marketing-enterprises-caffeine-powder-recall-unapproved-drug-risk. Based on FDA recall #D-1096-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1096-2017%22&limit=1).
Why it’s dangerous
The product is unapproved by the FDA as a drug because it makes stimulant claims without an approved application. It also lacks clear instructions for safe use, which could lead to misuse or health risks.
Who’s affected
People who purchased the caffeine powder from retailers like LifeLine Nutrients Corp. are affected. Those using it for medical purposes without proper approval are at higher risk.
How to tell if you have this one
Check for the product name 'Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz).' Look for batch numbers 15121931 or 15121939 and expiration date 12/19.
- Brand
Global Marketing Enterprises- Product
Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz)., 1250 servings, Packed By:- Category
Drug
What to do — step by step
Check Product Details
Identify the product name, batch numbers, and expiration date to confirm if it's recalled.
Questions people ask
Is this caffeine powder safe to use?
The product is unapproved by the FDA and lacks proper labeling, so it's not safe for intended use without approval.
How can I tell if I have the recalled product?
Check for the product name 'Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz).' with batch numbers 15121931 or 15121939 and expiration date 12/19.
What should I do if I have the recalled product?
The recall record does not specify a remedy, so contact Global Marketing Enterprises for guidance.
Contact Global Marketing Enterprises
We’ve drafted a message you can send Global Marketing Enterprises to request your refund or repair — edit it as you like.
Subject: Recall D-1096-2017 — Global Marketing Enterprises Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, Hello, I own a Caffeine Powder, Anhydrous, Pharmaceutical Grade, 100% Pure caffeine, 250 g (8.8 oz)., 1250 servings, Packed By: that is covered by recall D-1096-2017 from Global Marketing Enterprises. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1096-2017 (May 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1096-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.