ProSupps Recalls Mr. Hyde Green Apple Supplements Due to Mislabeling
ProSupps USA LLC is recalling 28,045 units of Mr. Hyde Green Apple supplements because they contain 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 typically involves a temporary or medically reversible adverse health consequence. The hazard is mislabeling involving a non-dietary ingredient, which fits the criteria for moderate severity without reported serious injuries or fatalities.
Plain-English summary
ProSupps USA LLC is recalling 28,045 units of Mr. Hyde Green Apple and Mr. Hyde Green Apple Sweden supplements. The recall was initiated because the products are potentially mislabeled and contain the non-dietary ingredient Picamilon.
The affected products were distributed in the United States and Canada. The specific lot codes involved in this recall are A107151015 and A109880116.
Consumers who have purchased these products should check their lot codes against the information provided. If the products match the recalled items, consumers should stop using them and contact the recalling firm for further instructions.
The recalled product
- Product
- Mr. Hyde Green Apple; Mr. Hyde Green Apple Sweden
- Manufacturer
- ProSupps USA LLC
- Category
- Food — Dietary Supplements
- Affected units
- 28,045
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 (2)
- A107151015
- A109880116
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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