FDA recall record

World Health Products GAT SPORT JETFUEL DIURETIC recall — FDA F-0522-2022

Product may contain undeclared milk.

Class IIclassification
F-0522-2022official record ID
Feb 2, 2022report date

Recall record at a glance

Official recordF-0522-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmWorld Health Products LLC
Report dateFeb 2, 2022
Recall initiation dateJan 6, 2022
Quantity3,838 units
LocationMonroe, CT, United States

Official product description

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)

Why the product was recalled

Product may contain undeclared milk.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.