The Recall Desk
ModerateFDA (Food)·F-1639-2015·Announced 2015-04-08

Health One Pharmaceuticals Recalls Shu Chang Bao Capsules for cGMP Violations

Health One Pharmaceuticals is recalling Shu Chang Bao capsules due to significant violations of dietary supplement 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 high-risk pathogens, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Health One Pharmaceuticals is voluntarily recalling Shu Chang Bao capsules. 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 recalled product consists of 60,000 units of Shu Chang Bao capsules. The distribution pattern includes nationwide sales in the United States, specifically in California, Tennessee, Washington, and Idaho, as well as international distribution to Hong Kong, Vietnam, China, and Singapore. The specific code information associated with the recall is 9756.

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

The recalled product

Product
Shu Chang Bao_A, capsule
Affected units
60,000

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)

  • 9756

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 →