Truvy 30-Day Experience Kit
Reported: May 31, 2023 Initiated: April 27, 2023 #F-0946-2023
Product Description
Truvy 30-Day Experience Kit
Reason for Recall
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Details
- Recalling Firm
- TruVision Health LLC
- Units Affected
- 9,693 packs
- Distribution
- 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
- Location
- Draper, UT
Frequently Asked Questions
What product was recalled? ▼
Truvy 30-Day Experience Kit. Recalled by TruVision Health LLC. Units affected: 9,693 packs.
Why was this product recalled? ▼
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 31, 2023. Severity: Moderate. Recall number: F-0946-2023.
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