Regeneca Recalls RegeneArouse Supplements for Manufacturing Violations
VivaCeuticals is recalling all lots of RegeneArouse herbal and dietary supplements because they were not manufactured in compliance with current Good Manufacturing Practice regulations.
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 and involves a manufacturing compliance issue (cGMP) without reported illnesses or specific high-risk pathogens, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
VivaCeuticals, Inc. dba Regeneca Worldwide is voluntarily recalling all lots of RegeneArouse herbal and dietary supplements. The recall is being conducted because the products were not manufactured in compliance with the current Good Manufacturing Practice (cGMP) regulations for Dietary Supplements.
The recall covers all lots of the product distributed in the United States. The source text does not specify the exact quantity of units affected or the specific distribution channels.
Consumers who have purchased RegeneArouse should stop using the product and contact the recalling firm for further instructions or a refund.
The recalled product
- Product
- RegeneArouse
- Manufacturer
- VivaCeuticals, Inc. dba Regeneca Worldwide
- Category
- Food — Dietary Supplements
- Hazard
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)
- all lots
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 7 recalled by VivaCeuticals, Inc. dba Regeneca Worldwide 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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