GM Manufacturing Recalls Ginseng Power Blister Packs for cGMP Violations
GM Manufacturing is recalling 3,025 units of Ginseng Power Blister Packs 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 cGMP violations without reported illnesses or specific high-risk pathogens, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
GM Manufacturing Inc. is recalling 3,025 units of Ginseng Power, Blister Packs. 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 in California. No specific lot numbers are provided for this recall. The U.S. Food and Drug Administration has classified this recall as Class II.
Consumers who have purchased this product should stop using it and contact GM Manufacturing Inc. for further instructions or a refund.
The recalled product
- Product
- Ginseng Power, Blister Packs
- Manufacturer
- GM Manufacturing Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 3,025
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)
- No Lot numbers
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 46 recalled by GM Manufacturing 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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