FDA recall record
Hikari Enjuku Koji Miso Mutenka; 26.6 oz. plastic tub with lid. UPC 4 905663 003007
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 7, 2019. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Hikari Enjuku Koji Miso Mutenka; 26.6 oz. plastic tub with lid. UPC 4 905663 003007
Reason
Miso product manufactured in Japan was distributed in US with no English labeling and therefore soy beans not properly declared on label as an allergen.
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.
Hikari Enjuku Koji Miso Mutenka; 26.6 oz. plastic tub with lid. UPC 4 905663 003007
Code information listed by FDA
Best Before 28.OCT. 2019
Distribution and firm information
Recalling firm listed by FDA: Hikari Miso International, Inc.
Firm location listed by FDA: Torrance, CA, United States
Distribution reported by FDA: One distributor in CA only
Product quantity listed by FDA: 224 cases ( 8 tubs per case)
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.