Basic Reset Recalls Beta Factor Dietary Supplement for CGMP Violations
Basic Reset Inc. is recalling 262 bottles of Beta Factor dietary supplement because the product does not conform to Dietary Supplement 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 due to non-conformance with CGMP regulations, which typically indicates a moderate risk of temporary or medically reversible health consequences without reported serious injuries or fatalities.
Plain-English summary
Basic Reset Inc. is recalling 262 bottles of Beta Factor Dietary Supplement, 60 capsules per plastic bottle (SKU: 100-4F). The recall was initiated because the products do not conform to Dietary Supplement Current Good Manufacturing Practice (CGMP) regulations.
The affected product was shipped to all 50 states and to foreign consignees in Canada, Nigeria, the U.K., Australia, Israel, Puerto Rico, the Virgin Islands, Hungary, the UAE, Mexico, the Philippines, and Greece. Specific lot codes associated with the recall include 1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, and W0003878.
Consumers who have purchased this product should stop using it and contact Basic Reset Inc. for further instructions or a refund. The FDA classifies this recall as Class II, indicating that use of the product could cause temporary or medically reversible health consequences.
The recalled product
- Product
- BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
- Manufacturer
- Basic Reset Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 262
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 (9)
- 1820705
- 1806004
- 1733404
- 1815204
- 1719204
- W0002670
- W0000304
- W000325
- W0003878
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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