Severity
Moderate
ModerateClass IIOngoing
FDA Food recall · Reported May 31, 2023
TruBoost 7 Day Experience Kit
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
TruVision Health LLC recalled TruBoost 7 Day Experience Kit - a moderate-severity action.
TruBoost 7 Day Experience Kit was recalled by TruVision Health LLC in May 31, 2023. Reason: The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.. Check the official notice for the remedy. Verify recall #F-0949-2023 with the FDA Food before acting.
The recall
TruVision Health LLC issued this moderate-severity FDA Food recall-The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients..
- Moderate
- severity level
- Class II
- classification
- May 31, 2023
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-0949-2023 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-0949-2023) was formally reported on May 31, 2023, with the manufacturer initiating the action on April 27, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. TruVision Health LLC is listed as the recalling firm, operating out of Draper, UT. Federal records list the affected scope as 14,510 packs.
The documented reason for this recall is: The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients. Distribution data in the federal record shows the product reached: 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 …. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
14,510 packs
Related Recalls
6
6 from same agency
Product description
TruBoost 7 Day Experience Kit
Reason for recall
The products contain DMHA and/or hordenine which FDA has determined are not acceptable dietary ingredients.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | F-0949-2023 |
| Date reported | May 31, 2023 |
| Date initiated | April 27, 2023 |
| Recalling firm | TruVision Health LLC |
| Firm location | Draper, UT |
| Affected scope | 14,510 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 Nev… |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-0949-2023) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
TruBoost 7 Day Experience Kit. Recalled by TruVision Health LLC. Units affected: 14,510 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-0949-2023.
Where was the recalled product distributed? ▼
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.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-0949-2023) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
FDA Food Critical
Blue Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Ent…
Pure Vitamins and Natural Supplements, LLC · 2026-04-15
FDA Food Critical
Red Bull Extreme Male Enhancement Supplement, total of 15 pouches per box, Net Wt 15 G each pouch. Dosage: Consume Enti…
Pure Vitamins and Natural Supplements, LLC · 2026-04-15
FDA Food Moderate
Bulk packaged Colustrum Powder. packaged with generic product label.
Herbal Creations USA · 2026-04-01
FDA Food Low
Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; N…
Winder Laboratories, LLC · 2026-03-25
FDA Food Moderate
Imu-Tek Immuno-5 Colostrum Powder 7 oz. Intended Use: Dietary Supplement for People. (Some customers use this for t…
Imu-Tek Animal Health, Incorporated · 2026-02-11
Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported May 31, 2023. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.