The Recall Desk
HighFDA (Food)·F-3597-2017·Announced 2017-10-11

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.

What this means for you

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
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 →