Basic Reset Recalls Q-min Dietary Supplement for CGMP Non-Compliance
Basic Reset Inc. is recalling Q-min 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, but the source text explicitly states no illnesses or injuries have been reported. The hazard is a regulatory non-compliance (CGMP) rather than a specific pathogen or physical defect, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Basic Reset Inc. is voluntarily recalling Q-min, a dietary supplement sold in 50-capsule plastic bottles (SKU: 100-9B). The recall is being conducted because the products do not conform to Dietary Supplement Current Good Manufacturing Practice (CGMP) regulations. The specific lot code associated with this recall is 170801-BSC0462.
The affected product was shipped to all 50 U.S. 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 or a refund. The source text does not report any illnesses or injuries associated with this recall.
The recalled product
- Product
- Q-min, 50 capsules per plastic bottle, SKU: 100-9B
- 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 (1)
- 170801-BSC0462
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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