Health One Pharmaceuticals Recalls Arginine Dietary Supplements
Health One Pharmaceuticals is recalling Arginine 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 involves a reasonable probability that use may cause temporary or medically reversible health consequences. The source cites cGMP violations without reporting specific illnesses or injuries, fitting the Moderate severity criteria for regulatory compliance issues.
Plain-English summary
Health One Pharmaceuticals is recalling 309,000 units of Arginine dietary supplements. The recall is being conducted due to 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 products were also distributed worldwide in Hong Kong, Vietnam, China, and Singapore. The specific code information for the recalled units is 9191.
Consumers who have purchased these products should stop using them and contact Health One Pharmaceuticals for further instructions or a refund.
The recalled product
- Product
- Arginine
- Manufacturer
- Health One Pharmaceuticals Inc
- Category
- Food — Dietary Supplements
- Hazard
- Affected units
- 309,000
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)
- 9191
Distribution
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.
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