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Kobayashi Noodle U.S.A. recall — Product is distributed in 10lb bulk packaging. Brown cardboard box…
FDA (enforcement) · August 27, 2025 · Class II
- Kobayashi Noodle U.S.A. recalled Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label.… — an FDA enforcement event posted , classified Class II, covering 2 product entries.
- FDA-stated reason: Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Kobayashi Noodle U.S.A.
- Source ID
- 97436
FDA Enforcement Report search →
Product entries (2)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| H-0502-2025 | Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (16049) UPC: NONE Manufactured by: Kobayashi… | Lots: 911, 916, 919, 932, 935, 940, 945, 950 | CA |
| H-0503-2025 | Product is distributed in 10lb bulk packaging. Brown cardboard box with generic label. Raw Ramen Noodle HA #22W (4942) UPC: NONE Manufactured by: Kobayashi… | Lot#893, Lot#894, Lot#897, Lot#898, Lot#899, Lot#900, Lot#901, Lot#902, Lot#903, Lot#904,… | CA |
FDA enforcement entries have no per-recall public URL — verify via the FDA Enforcement Report search using the firm name or a recall number above.
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