The Recall Desk
ModerateFDA (Food)·F-1750-2015·Announced 2015-04-08

Health One Pharmaceuticals Recalls Pure Trans-Reveratol Supplements for cGMP Violations

Health One Pharmaceuticals is recalling 764 units of Pure Trans-Reveratol dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) 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 significant cGMP violations, which fits the 'Moderate' severity criteria for voluntary precautionary recalls or minor labeling/quality errors without reported illness.

Plain-English summary

Health One Pharmaceuticals Inc is voluntarily recalling 764 units of Pure Trans-Reveratol dietary supplements. The recall was initiated because the product was found to have significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements.

The affected product was distributed nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho. The company also distributed the product internationally to Hong Kong, Vietnam, China, and Singapore. The product code associated with the recall is 7899.

Consumers who have purchased this product should stop using it and contact Health One Pharmaceuticals Inc for further instructions or a refund. The recall is based on manufacturing compliance issues rather than a specific reported contamination or illness.

The recalled product

Product
Pure Trans-Reveratol
Affected units
764

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)

  • 7899

Distribution

Distributed nationwide across the United States.

The notice also names 4 states specifically:

Part of a larger recall action

This product is one of 147 recalled by Health One Pharmaceuticals Inc 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 147 products in this recall →