TruBoost Drink Citrine Spark Recalled for Prohibited Dietary Ingredients
TruVision Health LLC is recalling TruBoost Drink - Citrine Spark because it contains DMHA and/or hordenine, which the FDA has determined are not acceptable dietary ingredients. Consumers should not consume the product.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II recall for products containing unacceptable dietary ingredients (DMHA and hordenine) with potential health risks; however, no reported illnesses or injuries are mentioned in the source material, placing this at the High severity level.
Plain-English summary
TruVision Health LLC is recalling TruBoost Drink - Citrine Spark, a beverage product distributed across the United States and internationally, due to the presence of unacceptable dietary ingredients.
The product contains DMHA and/or hordenine, which the FDA has determined are not acceptable ingredients for dietary supplements and beverages. Approximately 1,789 packs of the affected product (Lot PM17921F1) have been identified.
Consumers who have purchased this product are advised not to consume it. The product was distributed across all US states and to Australia, Canada, England, Germany, Ireland, and New Zealand.
The recalled product
- Product
- TruBoost Drink - Citrine Spark
- Manufacturer
- TruVision Health LLC
- Affected units
- 1,789
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot PM17921F1
Distribution
Part of a larger recall action
This product is one of 12 recalled by TruVision Health LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 12 products in this recall →Related recalls
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