The Recall Desk
ModerateFDA (Food)·F-1766-2015·Announced 2015-04-08

Health One Pharmaceuticals Recalls U Liver Pro Dietary Supplement

Health One Pharmaceuticals is recalling U Liver Pro 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 cGMP violations without reported illnesses or specific acute hazards like pathogens or allergens, fitting the criteria for moderate severity.

Plain-English summary

Health One Pharmaceuticals is voluntarily recalling U Liver Pro, 60 capsules, 300mg, due to significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements. The recall involves 1,940 units of the product.

The affected product was distributed nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho, as well as internationally in Hong Kong, Vietnam, China, and Singapore. The product code is 9181.

Consumers who have purchased this product should stop using it and contact Health One Pharmaceuticals for further instructions or a refund.

The recalled product

Product
U Liver Pro, 60 capsules, 300mg
Affected units
1,940

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)

  • 9181

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 →