CLASS II Food recall · Reported 28 Jun 2017 · FDA Enforcement Report

GEC TNT Thermanite Dietary Supplement recalled by Genetic Edge Compounds

Genetic Edge Compounds is recalling GEC TNT Thermanite Dietary Supplement, distributed in 21 states. The recall was initiated on 22 May 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots remaining within expiry.

Quantity recalled8473 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-2384-2017
FDA event ID: 77278
Recalling firm: Genetic Edge Compounds, McKinney, TX
Brand: Gec Tnt
Classification: Class II
Status: Terminated
Recall initiated: 22 May 2017
FDA classified: 20 Jun 2017
Reported: 28 Jun 2017
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Foreign Material
Product category: Dietary Supplements

Timeline

22 May 2017	Recall initiated by company
20 Jun 2017	Classified by FDA	+29 days
28 Jun 2017	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains DMAA and Methylsynephrine.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

GEC TNT Thermanite 60 Capsules Dietary Supplement in clear plastic bottle, UPC: 689466706222.

Where it was distributed

AL, AR, CA, CO, FL, GA, IL, IN, KS, KY, LA, MO, NE, NY, OH, OK, PA, SC, TN, TX, WA

Alabama Arkansas California Colorado Florida Georgia Illinois Indiana Kansas Kentucky Louisiana Missouri Nebraska New York Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas

Questions about this recall

Is GEC TNT Thermanite Dietary Supplement recalled?

Yes. Genetic Edge Compounds recalled GEC TNT Thermanite Dietary Supplement on 22 May 2017. The recall is Class II and its status is Terminated. Recall number F-2384-2017.

Why was it recalled?

Product contains DMAA and Methylsynephrine.

Which lots are affected?

All lots remaining within expiry.

Where was it sold?

AL, AR, CA, CO, FL, GA, IL, IN, KS, KY, LA, MO, NE, NY, OH, OK, PA, SC, TN, TX, WA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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