ProSupps Recalls Dr. Jekyll Orange Burst Supplements for Unapproved Ingredient
ProSupps USA LLC is recalling Dr. Jekyll V2 Orange Burst supplements because they contain the unapproved ingredient picamilon.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically involves a temporary or medically reversible health risk. The source text does not report any illnesses or injuries, and the hazard is the presence of an unapproved ingredient rather than a high-risk pathogen or structural defect.
Plain-English summary
ProSupps USA LLC is voluntarily recalling approximately 65,195 units of Dr. Jekyll V2 Orange Burst Domestic 30 and Dr. Jekyll Orange Burst domestic sample packs. The recall is being conducted because the product contains the unapproved ingredient picamilon.
The affected products were distributed in the United States and Canada. Specific lot codes associated with the recall include A107911115, A110400216, and X016652L1.
Consumers who have purchased these products should stop using them and contact ProSupps USA LLC for further instructions or a refund.
The recalled product
- Product
- Dr. Jekyll V2 Orange Burst Domestic 30; Dr. Jekyll Orange Burst domestic sample packs
- Manufacturer
- ProSupps USA LLC
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 65,195
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 (3)
- A107911115
- A110400216
- X016652L1
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.
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