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FDA source record Class II Terminated

GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal Actives; 90 Oil-Infused Capsules; Dietary Supplement; Other I...

Recall Date: 2022-01-06 Recalling Firm: World Health Products LLC Record Ref: F-0522-2022

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal Actives; 90 Oil-Infused Capsules; Dietary Supplement; Other I... and names World Health Products LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: World Health Products LLC
  • Classification: Class II
  • Status: Terminated
  • Recall date: 2022-01-06
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Product Description & Identification

GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal Actives; 90 Oil-Infused Capsules; Dietary Supplement; Other Ingredients: Gelatin (Capsule), Dicalcium Phosphate, Microcrystalline Cellulose, Magnesium Stearate, Silicon Dioxide, Titanium Dioxice (color); Contains: Tree Nuts (Coconut)

Reason for Recall / Hazard Identified

Product may contain undeclared milk.

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Domestic: AL, AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MS, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, VA, WA, WI, WV International: India, Brunei, Albania, Venezuela, Aruba, UAE, Malaysia, UK, Mexico, Russia, "Latin America" - specific country not provided, Poland/EU

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0522-2022
Indexed update
2026-08-09 21:59:13 UTC
Official source
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