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