Kobayashi Noodle USA recalls 10lb bulk raw ramen noodles due to soy lecithin ingredient not being declared on packaging. This affects consumers with soy allergies.
Ramen Noodle package label does not declare Soy as the source for lecithin ingredient.
Kobayashi Noodle USA is recalling 10lb bulk raw ramen noodles (HA #22W) because the packaging does not list soy as the source for lecithin. This could pose a risk for people with soy allergies who might not be aware of the ingredient.
The ramen noodles contain lecithin derived from soy, but the packaging does not list soy as the source. This means individuals with soy allergies might unknowingly consume the product and experience an allergic reaction.
People with soy allergies who consume the recalled ramen noodles may be at risk. The recall affects consumers who bought the 10lb bulk packaging from stores selling raw ramen noodles.
Check for brown cardboard boxes with generic labels containing 'Raw Ramen Noodle HA #22W (16049)'. The product was sold in 10lb bulk packaging with lots 911, 916, 919, 932, 935, 940, 945, 950.
Look for the label that states 'Raw Ramen Noodle HA #22W (16049)' on brown cardboard boxes with generic labels.
The recall is because the packaging does not list soy as the source for lecithin, which could affect people with soy allergies.
The recall record does not specify a remedy, so no action is required beyond checking if you have the product.
If you have the recalled ramen noodles, check the packaging for the label and contact Kobayashi Noodle USA for further instructions.
We’ve drafted a message you can send Kobayashi Noodle to request your refund or repair — edit it as you like.
Subject: Recall H-0502-2025 — Kobayashi Noodle Kobayashi Noodle Hello, I own a Kobayashi Noodle that is covered by recall H-0502-2025 from Kobayashi Noodle. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
