The Recall Desk
ModerateFDA (Food)·F-1638-2015·Announced 2015-04-08

Health One Pharmaceuticals Recalls Nu Kang Bao Dietary Supplements

Health One Pharmaceuticals is recalling Nu Kang Bao dietary supplements due to significant violations of 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 corresponds to a moderate severity score when no specific injuries or illnesses are reported in the source text.

Plain-English summary

Health One Pharmaceuticals is voluntarily recalling approximately 100,000 units of Nu Kang Bao 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 affected products were distributed nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho. The supplements were also distributed internationally in Hong Kong, Vietnam, China, and Singapore. The specific code information for the recalled units is 9757.

Consumers who have purchased Nu Kang Bao dietary supplements should stop using the product and contact Health One Pharmaceuticals for further instructions or a refund. The recall is classified as FDA Class II, indicating that use of, or exposure to, the violative product may cause temporary or medically reversible adverse health consequences.

The recalled product

Product
Nu Kang Bao
Affected units
100,000

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)

  • 9757

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 →