The Recall Desk
ModerateFDA (Food)·F-1666-2015·Announced 2015-04-08

Health One Pharmaceuticals Recalls Kenbi Dietary Supplements for cGMP Violations

Health One Pharmaceuticals is recalling Kenbi 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, which typically indicates a situation where use of the product could cause temporary or medically reversible health consequences. The source cites cGMP violations without reporting specific illnesses or injuries, aligning with a Moderate severity rating.

Plain-English summary

Health One Pharmaceuticals is voluntarily recalling Kenbi dietary supplements. The recall is being conducted because the product was found to have significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements.

The recall involves 2,404 units of the product. Distribution was 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 9411.

Consumers who have purchased Kenbi dietary supplements should stop using the product and contact Health One Pharmaceuticals for further instructions or a refund.

The recalled product

Product
Kenbi
Manufacturer
Health One Pharmaceuticals Inc
Category
Food — Dietary Supplements
Hazard
Affected units
2,404

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)

  • 9411

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 →

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