TruVision Health LLC is recalling approximately 184,661 units of various Truvy and TruVision Health brand dietary supplements. The recall includes multiple products such as truCONTROL, reFORM, and Truvy Boost kits because they contain DMHA and/or hordenine, which are stimulants the FDA has determined are not acceptable dietary ingredients. These products were distributed across all 50 U.S. states and internationally to Australia, Canada, England, Germany, Ireland, and New Zealand. Consumers should stop using the affected supplements immediately.
The products contain DMHA and/or hordenine, which are stimulant ingredients that can lead to increased blood pressure, cardiovascular problems, or other serious health complications.
You have 2 options:
Quantity: 73,450 packs
Quantity: Unknown
Quantity: 2,535 packs
Quantity: 31,353 packs
Quantity: 4,182 packs
Quantity: 6,793 packs
Quantity: 9,693 packs
Quantity: 13,581 packs
Quantity: 22,125 packs
Quantity: 14,510 packs
Quantity: 1,789 packs
Quantity: 4,650 packs
Truvy Boost Capsules
reFORM energy accelerator drink bag
Truvy Boost Drink Mix
TruVision Tru Weight & Energy Capsules
TruVision truCONTROL capsules
TruVy Capsules, 60 Tru and 60 Vy Capsules
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · FDA Press Release · Raw API Response
openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.