Health One Pharmaceuticals Recalls Femanol Dietary Supplement for cGMP Violations
Health One Pharmaceuticals is recalling Femanol 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 and involves cGMP violations without reported illnesses or specific acute hazards like allergens or pathogens, fitting the criteria for moderate severity.
Plain-English summary
Health One Pharmaceuticals is voluntarily recalling Femanol, 60 capsules, 500mg, due to significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements. The recall involves 1,996 units of the product.
The affected product was distributed nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho, as well as internationally in Hong Kong, Vietnam, China, and Singapore. The product code associated with this recall is 9759.
Consumers who have purchased this product should stop using it and contact Health One Pharmaceuticals for further instructions or a refund. The recall is being conducted to ensure compliance with federal manufacturing standards.
The recalled product
- Product
- Femanol, 60 capsules, 500mg
- Manufacturer
- Health One Pharmaceuticals Inc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,996
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)
- 9759
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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