FDA recall record
Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (16049) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens...
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 6, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (16049) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens: Wheat, Egg
Reason
Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.
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.
Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (16049) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens: Wheat, Egg
Code information listed by FDA
Lots: 911, 916, 919, 932, 935, 940, 945, 950
Distribution and firm information
Recalling firm listed by FDA: Kobayashi Noodle U.S.A.
Firm location listed by FDA: Gardena, CA, United States
Distribution reported by FDA: CA
Product quantity listed by FDA: 945 cases
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.