RecallHawk
Class II Recall

Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (16049)

Kobayashi Noodle U.S.A.

Summary

The FDA issued a Class II for Product is distributed in 10lb bulk packaging. Brown cardboard box with generic by Kobayashi Noodle U.S.A.. Reason: Ramen Noodle package label does not declare Soy as the source for lecithin ingredient..

Details

Source

Food Recall

External ID

H-0502-2025

Action Date

2025-08-27

Status

Terminated

Category

food

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

Lot/Code Info: Lots: 911, 916, 919, 932, 935, 940, 945, 950

Quantity Affected: 945 cases

Reason for Recall

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

Distribution

CA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-08-05

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 90 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Kobayashi Noodle U.S.A. has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Kobayashi Noodle U.S.A.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Kobayashi Noodle U.S.A. have FDA actions?

Kobayashi Noodle U.S.A. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0502-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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