WHY THIS PRODUCT IS LISTED
Other / see reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Product description & recall reason
The recall record describes “reFORM”; the source reports: “The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.”
Based on the official recall record; packaging and sales claims have not been verified. Verify with the official source ↗
Identify the product
- Product description
- reFORM
- Brand
- Not supplied by this source
- Lot, batch, UPC & other codes
- Lot 34159
- Quantity
- 2,535 packs
Where it came from & where it went
- Recalling firm
- TruVision Health LLC
- Recalling firm address
- 172 E 14075 S; N/A; Draper; UT; 84020-5725; United States
- Product production / origin location
- Not supplied by this source
- Distribution — source wording
- Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming and Australia, Canada, England, Germany, Ireland, New Zealand
States identified in the source
Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, Wyoming
State matching is derived from the source’s distribution wording, which may be incomplete. The recalling company’s address is not used as the distribution location.
A recalling firm’s address is not necessarily where the food was grown or manufactured. Distribution can change; check the official notice.
The dates, separated
- Recall initiated
- Apr 27, 2023
- Notice published
- Not supplied
- Enforcement report
- May 31, 2023
- Agency classification
- May 25, 2023
- Source termination date
- Not supplied
- Last retrieved here
- Sep 28, 2026
FDA’s enforcement status is historical and may not reflect the current recall lifecycle. A terminated recall does not certify a product as safe.
Record provenance & interpretation
- Source identifier
- F-0942-2023
- Agency event identifier
- 92173
- Status as supplied (not live status)
- Ongoing
- Category assignment
- Inferred from product text; not an agency classification.
- State matching
- Official distribution wording; locations are extracted only from distribution evidence, not company addresses. Coverage may be incomplete.
- Source dataset date
- Sep 25, 2026