FDA recall record
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 19, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Reason
Products do not conform to Dietary Supplement CGMP regulations.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Code information listed by FDA
1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878
Distribution and firm information
Recalling firm listed by FDA: Basic Reset Inc.
Firm location listed by FDA: Hendersonville, TN, United States
Distribution reported by FDA: 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.
Product quantity listed by FDA: 262 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.