Basic Reset Recalls Mello-Tonin Dietary Supplement for CGMP Violations
Basic Reset Inc. is recalling Mello-Tonin dietary supplements because they do not conform to Dietary Supplement CGMP regulations. The product was distributed to all 50 states and several foreign countries.
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 due to CGMP non-conformance, which typically indicates a risk of temporary or medically reversible health consequences, fitting the Moderate severity criteria for regulatory compliance issues without reported acute illness.
Plain-English summary
Basic Reset Inc. is voluntarily recalling Mello-Tonin, a 2 fl. oz. glass bottle dietary supplement (SKU: 100-5C), because the products do not conform to Dietary Supplement Current Good Manufacturing Practice (CGMP) regulations. The recall includes products with codes 180209-BSC2354 and 170801-BSC2354.
The affected product was shipped to all 50 states. It was also shipped to foreign consignees in Canada, Nigeria, the U.K., Australia, Israel, Puerto Rico, the Virgin Islands, Hungary, the UAE, Mexico, the Philippines, and Greece.
Consumers who have purchased this product should stop using it and contact Basic Reset Inc. for further instructions. The FDA has classified this recall as Class II, indicating that use of the product could cause temporary or medically reversible health consequences.
The recalled product
- Product
- Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C
- Manufacturer
- Basic Reset Inc.
- Category
- Food — Dietary Supplement
- Hazard
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 (2)
- 180209-BSC2354
- 170801-BSC2354
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 14 recalled by Basic Reset 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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