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H-0502-2025Class II

Kobayashi Noodle U.S.A.

What this record is not

A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.

Recalling firm
Kobayashi Noodle U.S.A.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2025-08-27
Distribution
CA
Firm state
CA
Product quantity
945 cases
Initiated by
Voluntary: Firm initiated
Reason for recall

Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.

Product description

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 / lot info

Lots: 911, 916, 919, 932, 935, 940, 945, 950

Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →