The Recall Desk
ModerateFDA (Food)·F-1773-2015·Announced 2015-04-08

Health One Pharmaceuticals Recalls Vigerect Dietary Supplements

Health One Pharmaceuticals is recalling Vigerect 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 involves a temporary or medically reversible adverse health consequence. The source cites cGMP violations without reporting specific illnesses or injuries, aligning with a Moderate severity rating.

Plain-English summary

Health One Pharmaceuticals is recalling Vigerect dietary supplements. 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 units were 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. The recall involves 2,040 units with code 8523.

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

The recalled product

Product
Vigerect
Manufacturer
Health One Pharmaceuticals Inc
Category
Food — Dietary Supplement
Hazard
Affected units
2,040

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)

  • 8523

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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