Health One Pharmaceuticals Recalls Stem Alive Dietary Supplement
Health One Pharmaceuticals is recalling Stem Alive 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 remote possibility of temporary or medically reversible health consequences. 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 Stem Alive, 90 capsules, due to significant violations of the current Good Manufacturing Practice (cGMP) regulations for dietary supplements. The recall involves 30,000 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 the recall is 8671.
Consumers who have purchased this product should stop using it and contact Health One Pharmaceuticals for further instructions or a refund.
The recalled product
- Product
- Stem Alive, 90 capsules
- Manufacturer
- Health One Pharmaceuticals Inc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 30,000
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)
- 8671
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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