Product is distributed in
Reason Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.
Product is distributed in recall
Recalled by Kobayashi Noodle U.S.A. · Gardena, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (4942) UPC: NONE Manufactured by: Kobayashi Noodle USA Allergens: Wheat, Egg
Quantity: 2800 cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot#893, Lot#894, Lot#897, Lot#898, Lot#899, Lot#900, Lot#901, Lot#902, Lot#903, Lot#904, Lot#905, Lot#906, Lot#907, Lot#910, Lot#912, Lot#913, Lot#914, Lot#915, Lot#916, Lot#917, Lot#918, Lot#921, Lot#922, Lot#923, Lot#924, Lot#925, Lot#926, lot#927, Lot#928, Lot#929, Lot#930, Lot#933, Lot#934, Lot#936, Lot#937, Lot#938, Lot#939, Lot#940, Lot#942, Lot#943, Lot#946, Lot#947, Lot#948, Lot#949, Lot#951
Where it was sold
California
FDA's distribution note: CA
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Kobayashi Noodle U.S.A.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 5, 2025
- In FDA report of
- Aug 27, 2025
- Terminated
- Apr 6, 2026
- FDA recall number
- H-0503-2025 · event 97436
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.