Health One Pharmaceuticals Recalls Harmony Qi Dietary Supplement Tablets
Health One Pharmaceuticals is recalling Harmony Qi tablets 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 and involves a voluntary precautionary recall for manufacturing violations (cGMP) without reported illnesses or specific acute hazards like allergens or pathogens.
Plain-English summary
Health One Pharmaceuticals is voluntarily recalling 2,170 units of Harmony Qi, 90 Tablets, 500mg. 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 affected product was distributed nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho. It was also distributed internationally in Hong Kong, Vietnam, China, and Singapore. The specific code information for the recalled units is 8122.
Consumers who have purchased this product should stop using it and contact Health One Pharmaceuticals for further instructions or a refund. This recall is a precautionary measure to ensure compliance with federal manufacturing standards.
The recalled product
- Product
- Harmony Qi, 90 Tablets, 500mg
- Manufacturer
- Health One Pharmaceuticals Inc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 2,170
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)
- 8122
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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