Basic Reset Recalls SlimUp Dietary Supplement for CGMP Non-Compliance
Basic Reset Inc. is recalling SlimUp 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, which typically indicates a temporary or medically reversible health risk. The source text cites CGMP non-compliance without reporting specific illnesses or injuries, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Basic Reset Inc. is voluntarily recalling SlimUp, a dietary supplement sold in 60-capsule plastic bottles (SKU: 100-5B). The recall was initiated because the products do not conform to Dietary Supplement Current Good Manufacturing Practice (CGMP) regulations. The specific lot code associated with the recall is 170801-BSC2130.
The affected product was shipped to all 50 U.S. states. It was also distributed 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 the recalling firm for instructions on how to return the product or obtain a refund. No specific illnesses or injuries have been reported in the source text.
The recalled product
- Product
- SlimUp 60 capsules per plastic bottle, SKU: 100-5B
- 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-BSC2130
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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