BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Recalling firm: Basic Reset Inc.
Products do not conform to Dietary Supplement CGMP regulations.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 19, 2020.
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FDA code information
1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878
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Full FDA record and distribution details
Original product description
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Original FDA recall reason
Products do not conform to Dietary Supplement CGMP regulations.
Recall details
- Recall number
- F-0170-2020
- Event ID
- 83917
- FDA status
- Terminated
- Initiated
- Sep 23, 2019
- Reported
- Nov 27, 2019
- Classified
- Nov 21, 2019
- Terminated
- Aug 19, 2020
- Quantity
- 262 bottles
- Location
- Hendersonville, TN, United States
- Initiation type
- FDA Mandated
- Notification
Where it was distributed
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.
Data updated September 16, 2026. View official FDA data ↗
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