CLASS II ONGOING Food recall · Reported 31 May 2023 · FDA Enforcement Report
TruBoost 7 Day Experience Kit recalled by TruVision Health
TruVision Health is recalling TruBoost 7 Day Experience Kit, distributed in 50 states. The recall was initiated on 27 Apr 2023 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0949-2023
- FDA event ID
- 92173
- Recalling firm
- TruVision Health, Draper, UT
- Brand
- TruBoost
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 27 Apr 2023
- FDA classified
- 25 May 2023
- Reported
- 31 May 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Other Reasons
- Product category
- Ready Meals
Timeline
| 27 Apr 2023 | Recall initiated by company | |
| 25 May 2023 | Classified by FDA | +28 days |
| 31 May 2023 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Product as listed by the FDA
TruBoost 7 Day Experience Kit
Where it was distributed
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
AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMaryland
Questions about this recall
Is TruBoost 7 Day Experience Kit recalled?
Yes. TruVision Health recalled TruBoost 7 Day Experience Kit on 27 Apr 2023. The recall is Class II and its status is Ongoing. Recall number F-0949-2023.
Why was it recalled?
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Which lots are affected?
Lot 13985
Where was it sold?
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
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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