Health One Pharmaceuticals Recalls Ultra Lecithin Dietary Supplements
Health One Pharmaceuticals is recalling Ultra Lecithin 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 injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Health One Pharmaceuticals Inc is recalling 2,400 units of Ultra Lecithin 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 products were distributed nationwide in the United States, specifically in California, Tennessee, Washington, and Idaho. The company also distributed the product internationally to Hong Kong, Vietnam, China, and Singapore. The specific code information associated with the recalled units is 112121.
Consumers who possess this product should stop using it and contact Health One Pharmaceuticals Inc for further instructions or a refund. The source text does not report any specific illnesses or injuries associated with this recall.
The recalled product
- Product
- Ultra Lecithin
- Manufacturer
- Health One Pharmaceuticals Inc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 2,400
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)
- 112121
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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