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) recalled over Undeclared allergen
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:
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. The Food and Drug Administration (FDA) laboratory analysis has found Lipofit Extreme Fat Burner 2.0 to
- Hazard class
- Class II — possible temporary or reversible harm
- Recalling company
- Ana Salazar Modela Tu Cuerpo Inc.
- Recall type
- Voluntary
- Quantity
- Distribution
Frequently asked questions
Is 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) recalled?
Yes. It was recalled on August 27, 2026 because 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. The Food and Drug Administration (FDA) laboratory analysis has found Lipofit Extreme Fat Burner 2.0 to
What should I do if I have it?
Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Which states are affected?
This recall is nationwide.
How do I identify the recalled product?
Look for: .
How serious is a Class II recall?
Class II means possible temporary or reversible harm.
Get recalls in your inbox
One short email whenever a new U.S. food recall is posted. Free. Unsubscribe anytime.
Want alerts only for your allergens or brands? Build a watchlist →