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Basic Reset Inc.
FDA recall F-0170-2020 · Class II · reported 2019-11-27 · Terminated
- Product
- BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
- Reason
- Products do not conform to Dietary Supplement CGMP regulations.
- Quantity
- 262 bottles
- Distribution
- Product was shipped to all 50 states. Product was shipped to the following foreign consignees: Canada, Nigeria, U.K., Australia, Israel, Puerto Rico, Virgin Islands, Hungary, UAE, Mexico, Philippines, Greece, and Puerto Rico.
- Firm location
- TN, United States
- Initiated
- FDA Mandated
- First notice
- Recall started
- 2019-09-23
- Terminated
- 2020-08-19
- Code info
- 1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.