FDA-ordered recall of Lipofit Extreme Fat Burner after toxic chemicals found
A nationwide recall was launched for Lipofit Extreme Fat Burner 2.0 after the FDA detected undeclared fluoxetine and the hazardous pesticide 2,4-Dinitrophenol in the product.
Ana Salazar Modela Tu Cuerpo Inc., a Florida-based firm, issued a nationwide recall of its Lipofit Extreme Fat Burner 2.0 after laboratory analysis by the Food and Drug Administration revealed the presence of undeclared fluoxetine in the daytime tablets and the toxic pesticide 2,4-Dinitrophenol (DNP) in the nighttime tablets. The FDA had previously cautioned shoppers in June not to buy the supplement because both substances are barred from dietary products and can trigger life-threatening symptoms such as cardiac arrhythmia, rapid heart rate, and sudden death.
The affected batches carry lot number 25M12F and are marked to expire in September 2027; they were distributed directly to consumers via online sales. Although the company has not received any reports of injuries linked to the product, it advises anyone who purchased the supplement to cease use immediately, keep it away from children, and follow specific return or disposal directions. Potential health risks include nausea, vomiting, dizziness, seizures, vision loss, and severe overheating, especially when combined with certain medications. Consumers experiencing any related symptoms are urged to seek medical advice.
Why it matters
The recall protects consumers from a supplement containing a banned pesticide that can cause serious, potentially fatal health problems.
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