FDA Food recall F-0949-2023
TruBoost 7 Day Experience Kit
- FDA Food
- Class II
- ongoing
- Published 2023-05-31
On 2023-05-31 the FDA classified a Class II recall of TruBoost 7 Day Experience Kit by Truvision Health, citing the products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-0949-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-04-27 |
| Published | 2023-05-31 |
| Last updated | 2026-09-13 11:50 UTC |
| Company | Truvision Health |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
TruBoost 7 Day Experience Kit
Reason
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Identifiers
| code_info | Lot 13985 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:50 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0949-2023%22
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