Class II
FDA
Lipofit Extreme Fat Burner 2.0 recalled over Undeclared drug ingredient
Lipofit Extreme Fat Burner 2.0 was recalled on August 27, 2026 because of undeclared drug ingredient. It is a Class II recall (possible temporary or reversible harm). Affected area: nationwide. Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
HazardUndeclared drug ingredient
Risk levelClass II
Affected areaNationwide
CategoryFood
What to do
Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Confirm the details against the official FDA notice before acting.
Does this affect you?
Check the product in your home against the recalled item:
- Product as filed
- Ana Salazar Modela Tu Cuerpo Inc. — Nationwide Voluntary Recall of Lipofit Extreme Fat Burner 2.0 Due to Presence of Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)
- Lot & date codes
- 25M12F
Full recall details
- Reason for recall
- FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.
- Hazard class
- Class II — possible temporary or reversible harm
- Recalling company
- Ana Salazar Modela Tu Cuerpo Inc.
- Recall type
- Voluntary
- Quantity
- Distribution
- Risk Statement: Lipofit Extreme 2.0 Fat Burner, is a product promoted and sold for weight loss. The product was distributed in the United States directly to individual consumers through online sales.
Compiled from the official FDA record by our data rules — how we build these pages. Spotted an error? Report it.
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