VivaCeuticals Recalls RegeneBlast Supplements for Manufacturing Violations
VivaCeuticals is recalling all lots of RegeneBlast 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, which typically involves a reasonable probability of temporary or medically reversible health consequences. The source text cites non-compliance with Good Manufacturing Practices but does not report specific illnesses, injuries, or high-risk pathogens, aligning with a Moderate severity rating.
Plain-English summary
VivaCeuticals, Inc. dba Regeneca Worldwide is recalling all lots of RegeneBlast 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. The source text does not specify the quantity of units affected or the specific distribution locations beyond the general product description.
Consumers who have purchased RegeneBlast should stop using the product and contact the recalling firm for further instructions.
The recalled product
- Product
- RegeneBlast
- 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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