FDA recall record
Keto Living Sugar Control
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 April 30, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Keto Living Sugar Control
Reason
Contains undeclared wheat (gluten) in product labeled "gluten free"
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.
Keto Living Sugar Control
Code information listed by FDA
Product Code 82004 with lot codes 1362073 and 1365200 Product Code: Ue82004 with lot codes 1361754 and 1364325
Distribution and firm information
Recalling firm listed by FDA: Natural Organics, Inc.
Firm location listed by FDA: Melville, NY, United States
Distribution reported by FDA: Nationwide; United Arab Emirates, Kenya, Spain, Trinidad, and the United Kingdom.
Product quantity listed by FDA: 4,650 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.