Kobayashi Noodle USA recalls 10lb bulk raw ramen noodles (HA #22W) due to missing soy lecithin ingredient label. This may affect people 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 product label does not state that soy is the source of lecithin. This could be a problem for people with soy allergies who rely on ingredient labels to avoid allergens.
The ramen noodles do not list soy as the source of lecithin on the label. This could lead to unintended exposure for individuals with soy allergies who need to avoid this ingredient. The hazard is related to labeling accuracy, not physical harm.
People who have soy allergies or are sensitive to soy products may be affected. The recall covers specific lot numbers of raw ramen noodles sold in bulk packaging.
Check for brown cardboard boxes with generic labels containing 'Raw Ramen Noodle HA #22W (4942)'. The product was sold in 10lb bulk packaging with specific lot numbers listed in the recall.
Look for the label stating 'Soy' as the source of lecithin ingredient on the product packaging.
The recall indicates the label does not declare soy as the source of lecithin, which could be a concern for people with soy allergies. However, the product itself may still be safe if the soy source is not present.
The affected lot numbers are 893 through 951, as listed in the recall notice.
Check for brown cardboard boxes with generic labels containing 'Raw Ramen Noodle HA #22W (4942)' in 10lb bulk packaging.
We’ve drafted a message you can send Kobayashi Noodle to request your refund or repair — edit it as you like.
Subject: Recall H-0503-2025 — Kobayashi Noodle Kobayashi Noodle Hello, I own a Kobayashi Noodle that is covered by recall H-0503-2025 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.
