Ottogi America recalls 5-pack snack ramen due to undeclared egg allergen. Consumers should check product codes and avoid if allergic to egg.
Undeclared allergen; egg.
Ottogi America is recalling snack ramen products that contain undeclared egg, a known allergen. This poses a risk for people with egg allergies who could experience an allergic reaction. Read more at govinfonow.com/recall/17818-ottogi-snack-ramen-5pk-recall-undeclared-egg-allergen-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/17818-ottogi-snack-ramen-5pk-recall-undeclared-egg-allergen-hazard · Updated October 5, 2026 · FDA enforcement record: FDA #F-1063-2019
“Ottogi Snack Ramen 5PK Recall: Undeclared Egg Allergen Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17818-ottogi-snack-ramen-5pk-recall-undeclared-egg-allergen-hazard. Based on FDA recall F-1063-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1063-2019%22&limit=1).
The ramen contains egg without being listed on the label. This can cause an allergic reaction in people who are sensitive to egg, potentially leading to symptoms like hives, swelling, or difficulty breathing.
People with egg allergies are at risk of an allergic reaction if they consume the recalled ramen. The product is sold in the U.S. through Ottogi America.
Check for product codes 21501281 or 21502161 on the packaging. The ramen was sold between January 2019 and November 2019.
Look for product codes 21501281 or 21502161 on the packaging.
Yes, the recall is only for people with egg allergies. The product contains egg but is safe for others.
The ramen was sold from January 2019 to November 2019.
Check the product codes on the packaging and avoid if you have an egg allergy.
We’ve drafted a message you can send Ottogi to request your refund or repair — edit it as you like.
Subject: Recall F-1063-2019 — Ottogi Ottogi Hello, I own a Ottogi that is covered by recall F-1063-2019 from Ottogi. 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.
