ProSupps Recalls Dr. Jekyll V2 Orange Burst for Undeclared Ingredient
ProSupps USA LLC is recalling 698 units of Dr. Jekyll V2 Orange Burst because the product is potentially mislabeled and contains the non-dietary 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 2/5 (Moderate).
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 corresponds to a moderate severity score of 2 in the absence of reported illnesses or injuries.
Plain-English summary
ProSupps USA LLC is recalling 698 units of Dr. Jekyll V2 Orange Burst. The recall is being conducted because the product is potentially mislabeled and contains the non-dietary ingredient Picamilon.
The affected product was distributed in the US and Canada. The specific code for the recalled units is A109850116.
Consumers who have purchased this product should check their inventory for the specific code and stop using the product if it matches the recalled description.
The recalled product
- Product
- Dr. Jekyll V2 Orange Burst domestic
- Manufacturer
- ProSupps USA LLC
- Category
- Food — Dietary Supplement
- Affected units
- 698
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)
- A109850116
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 8 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 8 products in this recall →Related recalls
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Similar recalls
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