ProSupps Recalls Hyde V2 Orange Burst for Unapproved Ingredient
ProSupps USA LLC is recalling Hyde V2 Orange Burst dietary supplements because they contain the unapproved ingredient picamilon.
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: The recall is classified as FDA Class II, and the presence of an unapproved ingredient in a dietary supplement represents a risk of harm where specific injury reports are not detailed in the source text.
Plain-English summary
ProSupps USA LLC is voluntarily recalling approximately 2,147 units of Hyde V2 Orange Burst dietary supplements. The recall was initiated because the product contains picamilon, an ingredient that is not approved for use in dietary supplements.
The affected products were distributed in the United States and Canada. The specific code associated with the recalled units is A109151215.
Consumers who possess this product should stop using it and contact the manufacturer for further instructions or a refund.
The recalled product
- Product
- Hyde V2 Orange Burst
- Manufacturer
- ProSupps USA LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 2,147
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)
- A109151215
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 18 recalled by ProSupps USA 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 18 products in this recall →Related recalls
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