ProSupps Recalls Green Apple Supplement Containing Unapproved Ingredient
ProSupps USA LLC is recalling Dr. Jekyll Green Apple V2 domestic because it contains 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 adverse health consequence. The source text does not report specific injuries or illnesses, aligning with a moderate severity rating for an unapproved ingredient recall without reported harm.
Plain-English summary
ProSupps USA LLC is recalling 1,827 units of Dr. Jekyll Green Apple V2 domestic. The product was distributed in the US and Canada.
The recall was initiated because the product contains the unapproved ingredient picamilon. The specific lot code associated with this recall is RLA105850815.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Dr. Jekyll Green Apple V2 domestic
- Manufacturer
- ProSupps USA LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,827
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)
- RLA105850815
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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