RegeneFit Dietary Supplements Recalled for Manufacturing Non-Compliance
VivaCeuticals is recalling RegeneFit 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 the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity recall involving regulatory non-compliance without immediate health consequences.
Plain-English summary
VivaCeuticals, Inc. dba Regeneca Worldwide is recalling RegeneFit herbal and dietary supplements. The recall involves 300 units of the product, specifically lot B1109329, which were distributed in the United States.
The firm is recalling the product because it was not manufactured in compliance with the current Good Manufacturing Practice (cGMP) regulations for Dietary Supplements. These regulations are designed to ensure that dietary supplements are safe, pure, and accurately labeled.
Consumers who have purchased RegeneFit should stop using the product. The source text does not provide specific instructions for disposal or return, nor does it report any illnesses or injuries associated with the recall.
The recalled product
- Product
- RegeneFit
- Manufacturer
- VivaCeuticals, Inc. dba Regeneca Worldwide
- Category
- Food — Dietary Supplements
- Affected units
- 300
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 B1109329
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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