FDA recall record
Havasu Beetroot Powder, 11.5 oz.
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 June 26, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Havasu Beetroot Powder, 11.5 oz.
Reason
Contains undeclared milk
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.
Havasu Beetroot Powder, 11.5 oz.
Code information listed by FDA
Lot # 111-2023021 and Best by date, January 2026 UPC: X002H69359
Distribution and firm information
Recalling firm listed by FDA: Supplement Manufacturing Partner, Inc.
Firm location listed by FDA: Edgewood, NY, United States
Distribution reported by FDA: Amazon nationwide; Shopify nationwide
Product quantity listed by FDA: 1,501 units
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.