RegeneSlim herbal supplement recalled for manufacturing non-compliance
VivaCeuticals is recalling RegeneSlim 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 injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
VivaCeuticals, Inc. dba Regeneca Worldwide is recalling RegeneSlim herbal and dietary supplements. The recall involves 4,000 units of the product, specifically Lot AAMXG, which were distributed in the United States.
The firm is recalling these products because they were not manufactured in compliance with the current Good Manufacturing Practice (cGMP) regulations for Dietary Supplements. The source text does not report any specific illnesses, injuries, or deaths associated with the product.
Consumers who have purchased RegeneSlim should check their lot numbers. If they possess Lot AAMXG, they should stop using the product and contact the recalling firm for further instructions.
The recalled product
- Product
- RegeneSlim
- Manufacturer
- VivaCeuticals, Inc. dba Regeneca Worldwide
- Category
- Food — Dietary Supplement
- Affected units
- 4,000
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)
- Lot AAMXG
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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