Genetic Edge GEC TNT Thermanite 60 Capsules Recall: DMAA and Methylsynephrine Hazard
Genetic Edge recalls 60-capsule dietary supplement containing DMAA and Methylsynephrine. This product may pose health risks. Consumers should check UPC 689466706222 for affected items.
Recall notice
Product contains DMAA and Methylsynephrine.
Contact the company
What happened, in plain English
Genetic Edge is recalling 60-capsule dietary supplements that contain DMAA and Methylsynephrine. These ingredients may cause health risks, so affected consumers should stop using the product. Read more at govinfonow.com/recall/21174-genetic-edge-gec-tnt-thermanite-60-capsules-recall-dmaa-and.
Source Summary by GovInfoNow · govinfonow.com/recall/21174-genetic-edge-gec-tnt-thermanite-60-capsules-recall-dmaa-and · Updated October 8, 2026 · FDA enforcement record: FDA #F-2384-2017
Cite this page
“Genetic Edge GEC TNT Thermanite 60 Capsules Recall: DMAA and Methylsynephrine Hazard.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21174-genetic-edge-gec-tnt-thermanite-60-capsules-recall-dmaa-and. Based on FDA recall #F-2384-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2384-2017%22&limit=1).
Why it’s dangerous
The product contains DMAA and Methylsynephrine, which are stimulants that can cause health issues such as increased heart rate, blood pressure, and potential adverse reactions. These ingredients are not approved for use in dietary supplements by the FDA.
Who’s affected
Anyone who owns or uses the GEC TNT Thermanite 60 Capsules Dietary Supplement in clear plastic bottle with UPC 689466706222. People most at risk are those who have taken the product without knowing it contains these ingredients.
How to tell if you have this one
Check for the product name 'GEC TNT Thermanite 60 Capsules Dietary Supplement' in a clear plastic bottle with UPC 689466706222. All lots within the expiry date are affected.
- Brand
Genetic Edge- Product
GEC TNT Thermanite 60 Capsules Dietary Supplement in clear plastic bottle, UPC: 689466706222- Category
Food
What to do — step by step
Check Product Details
Look for the UPC 689466706222 on the clear plastic bottle to confirm if you have the recalled product.
Where it went and when
Where it was distributed
Distributed in 21 states.
FDA distribution: “AL, AR, CA, CO, FL, GA, IL, IN, KS, KY, LA, MO, NE, NY, OH, OK, PA, SC, TN, TX, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arkansas, California, Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Kentucky, Louisiana, Missouri, Nebraska, New York, Ohio, Oklahoma, Pennsylvania, South Carolina, Tennessee, Texas, Washington.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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 #F-2384-2017 (May 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2384-2017 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.