ProSupps Recalls Dr. Jekyll Watermelon Supplements for Unapproved Ingredient
ProSupps USA LLC is recalling Dr. Jekyll 30 Watermelon and Dr. Jekyll Watermelon V2 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 corresponds to a Moderate severity score (2) in the absence of reported injuries or hospitalizations, as the hazard involves an unapproved ingredient without explicit reports of severe harm in the source text.
Plain-English summary
ProSupps USA LLC is voluntarily recalling approximately 34,387 units of Dr. Jekyll 30 Watermelon and Dr. Jekyll Watermelon V2 dietary supplements. The recall was initiated because the products contain picamilon, an ingredient that is not approved for use in dietary supplements.
The affected products were distributed in the United States and Canada. Specific lot codes associated with the recall include A107311015, A108371215, A111520316, and RLA103290615.
Consumers who have purchased these products should stop using them and contact ProSupps USA LLC for further instructions or a refund. The U.S. Food and Drug Administration (FDA) has classified this recall as Class II, indicating that use of the product could cause temporary or medically reversible health consequences.
The recalled product
- Product
- Dr. Jekyll 30 Watermelon; Dr. Jekyll Watermelon V2 domestic
- Manufacturer
- ProSupps USA LLC
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 34,387
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 (4)
- A107311015
- A108371215
- A111520316
- RLA103290615
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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