CLASS I Food recall · Reported 6 Mar 2019 · FDA Enforcement Report

Ottogi Snack Ramen, Cup x x 6ea recalled by Ottogi America

Ottogi America is recalling Ottogi Snack Ramen, Cup x x 6ea, distributed in 12 states. The recall was initiated on 15 Jan 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBEST BEFORE JAN.15.2019 to BEST BEFORE NOV.21.2019
Quantity recalled1,594,338 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1063-2019
FDA event ID
81944
Recalling firm
Ottogi America, Gardena, CA
Classification
Class I
Status
Terminated
Recall initiated
15 Jan 2019
FDA classified
22 Feb 2019
Reported
6 Mar 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Allergens
Product category
Pasta & Noodles

Timeline

15 Jan 2019Recall initiated by company
22 Feb 2019Classified by FDA+38 days
6 Mar 2019Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared allergen; egg.

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Ottogi Snack Ramen 5PK, Cup 1lb 3.05oz x 8pk, 2.18oz x 6ea Item #21501281, 21502161 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249

Where it was distributed

U.S. distribution to the following: CA, WA, UT, IL, TX, NJ, GA, NV, CO, HI, OR, AZ Foreign distribution to the following: Canada

ArizonaCaliforniaColoradoGeorgiaHawaiiIllinoisNew JerseyNevadaOregonTexasUtahWashington

Questions about this recall

Is Ottogi Snack Ramen, Cup x x 6ea recalled?

Yes. Ottogi America recalled Ottogi Snack Ramen, Cup x x 6ea on 15 Jan 2019. The recall is Class I and its status is Terminated. Recall number F-1063-2019.

Why was it recalled?

Undeclared allergen; egg.

Which lots are affected?

BEST BEFORE JAN.15.2019 to BEST BEFORE NOV.21.2019

Where was it sold?

U.S. distribution to the following: CA, WA, UT, IL, TX, NJ, GA, NV, CO, HI, OR, AZ Foreign distribution to the following: Canada

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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