Ana Salazar Modela Tu Cuerpo Inc. of Davie, Florida, is recalling Lipofit Extreme Fat Burner 2.0 nationwide after FDA laboratory analysis confirmed the product contains two undeclared substances: fluoxetine — a prescription antidepressant sold under the brand name Prozac — in the daytime (AM) tablets, and 2,4-dinitrophenol (DNP) — a toxic industrial chemical used as a pesticide, dye, and herbicide — in the nighttime (PM) tablets. Neither substance is listed on the product label. The recall was announced August 27, 2026. No adverse events have been reported to date, though the FDA had previously issued a safety advisory about this product on June 4, 2026.
What’s Being Recalled?
The recall covers Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, sold nationwide. The product is promoted and sold for weight loss as a dietary supplement at anasalazar.us.com and possibly at select retail locations. No other products are included in this recall.
Why Was This Product Recalled?
FDA laboratory testing found two hidden pharmaceutical and chemical substances in the product. The daytime (AM) tablets contain fluoxetine — a prescription-only FDA-approved antidepressant that is not approved for use as a weight-loss supplement. Fluoxetine can cause suicidal thoughts, abnormal bleeding, seizures, and dangerous heart rhythm problems, particularly when combined with other medications. The nighttime (PM) tablets contain DNP (2,4-dinitrophenol), an industrial toxic substance used as a pesticide, herbicide, and wood preservative that is NOT approved for human consumption. DNP is illegally marketed as a weight-loss compound and has caused multiple deaths. It raises body temperature to dangerous levels, causes rapid breathing, and can lead to cardiac arrest. When both substances are present together, the risk of fatal cardiac events is further elevated. Additional long-term risks include eye damage, bone marrow damage, and nervous system damage.
What Should You Do?
Stop taking Lipofit Extreme Fat Burner 2.0 immediately. Do not use any remaining product. Dispose of it safely and contact your healthcare provider — especially if you have been taking any other medications, as drug interactions with fluoxetine can be life-threatening. If you have experienced adverse symptoms including rapid heart rate, chest pain, difficulty breathing, unusual bleeding, or suicidal thoughts after taking this product, seek emergency medical care immediately and report it to the FDA’s MedWatch program at 1-800-332-1088 or fda.gov/safety/medwatch. Contact Ana Salazar Modela Tu Cuerpo at 954-289-3558 or [email protected].
