FDA recall record

Kobayashi Noodle U.S.A Product is distributed in 10lb bulk packaging recall — FDA H-0502-2025

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

Class IIclassification
H-0502-2025official record ID
Aug 27, 2025report date

Recall record at a glance

Official recordH-0502-2025
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKobayashi Noodle U.S.A.
Report dateAug 27, 2025
Recall initiation dateAug 5, 2025
Quantity945 cases
LocationGardena, CA, United States

Official 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

Why the product was recalled

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

Distribution information

CA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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