Home / TruVision Health LLC / F-0947-2023
Class IIOngoing

TruVision Health LLC

Recall #F-0947-2023 · Initiated 2023-04-27

Product
Truvy 7-Day Experience Kit
Reason for recall
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Quantity affected
13,581 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
Lot / code info
Lot 41404
Voluntary / mandated
Voluntary: Firm initiated
Initial notification
Press Release

Recalling firm

TruVision Health LLC
172 E 14075 S
Draper, UT 84020-5725
United States

Recall classification

Remote probability of serious adverse health consequences, or temporary reversible consequences.

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