World Health Products GAT SPORT JETFUEL DIURETIC Recall: Undeclared Milk Risk
World Health Products recalls GAT SPORT JETFUEL DIURETIC supplements due to potential undeclared milk content. Consumers should check lot numbers 2003610 and 2003609 for affected products.
Lower-risk recall
Product may contain undeclared milk.
Contact the company
What happened, in plain English
World Health Products is recalling GAT SPORT JETFUEL DIURETIC supplements because they may contain undeclared milk. This poses a risk for people with milk allergies who could experience allergic reactions. Read more at govinfonow.com/recall/13410-world-health-products-gat-sport-jetfuel-diuretic-recall-undeclared-milk.
Source Summary by GovInfoNow · govinfonow.com/recall/13410-world-health-products-gat-sport-jetfuel-diuretic-recall-undeclared-milk · Updated October 4, 2026 · FDA enforcement record: FDA #F-0522-2022
Cite this page
“World Health Products GAT SPORT JETFUEL DIURETIC Recall: Undeclared Milk Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13410-world-health-products-gat-sport-jetfuel-diuretic-recall-undeclared-milk. Based on FDA recall #F-0522-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0522-2022%22&limit=1).
Why it’s dangerous
The supplement may contain undeclared milk, which can trigger allergic reactions in individuals with milk allergies. This is a potential hazard for people who are allergic to dairy proteins.
Who’s affected
People who have milk allergies or are sensitive to dairy products are at risk. Those who purchased the specific lot numbers 2003610 and 2003609 are most likely affected.
How to tell if you have this one
Check the product label for lot numbers 2003610 or 2003609. The product is a dietary supplement sold under the brand name GAT SPORT JETFUEL DIURETIC.
- Brand
World Health Products- Category
Food
What to do — step by step
Check Product Label
Look for lot numbers 2003610 or 2003609 on the supplement packaging.
Where it went and when
Where it was distributed
Distributed in 39 states, and outside the U.S.
FDA distribution: “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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Nebraska, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Virginia, Washington, West Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 15 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-0522-2022 (January 6, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0522-2022 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.