The Recall Desk
ModerateFDA (Food)·F-1753-2015·Announced 2015-04-08

Health One Recalls Reishi Mushroom Capsules for cGMP Violations

Health One Pharmaceuticals is recalling Reishi Mushroom capsules due to significant violations of dietary supplement manufacturing 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 illnesses or injuries are reported in the source text.

Plain-English summary

Health One Pharmaceuticals Inc is voluntarily recalling 2,771 units of Reishi Mushroom, 90 capsules. 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, identified by code 9671, was distributed nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho. The product was also distributed internationally in Hong Kong, Vietnam, China, and Singapore.

Consumers who have purchased this product should stop using it and contact Health One Pharmaceuticals for further instructions or a refund. The recall is classified as FDA Class II, indicating that use of the product may cause temporary or medically reversible health consequences.

The recalled product

Product
Reishi Mushroom, 90 capsules
Manufacturer
Health One Pharmaceuticals Inc
Category
Food — Dietary Supplement
Hazard
Affected units
2,771

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)

  • 9671

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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