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Recall Number: F-0946-2023

Why was Truvy 30-Day Experience Kit recalled?

The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

Check out this page for guidance on what to do if you've consumed food from recall F-0946-2023 .

TruVision Health LLC recall in Draper, UT details
Here's recall specific data. Click on the company, city, or state for more recalls by TruVision Health LLC or more recalls in Draper or Utah.

  • City: Draper

  • State: Utah

  • Country: United States

  • Classification: Class II

  • Classification Date: 2023-05-25

  • Reason: The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.

  • Product Description: Truvy 30-Day Experience Kit

  • Report Date: 2023-05-31

  • Product Type: Food

  • Company: TruVision Health LLC

  • Status: Ongoing

  • Recall Number: F-0946-2023

  • Postal Code: 84020-5725

  • Recall Initiation Date: 2023-04-27

  • Recall End Date:

  • Event ID: 92173

  • Distribution Pattern: 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

  • Voluntary Or Mandated: Voluntary: Firm initiated

  • Initial Firm Notification: Press Release

  • Extra Info: Lot 39643/42825

  • Product Quantity: 9,693 packs

  • Address: 172 E 14075 S

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