VerifyRecall
Alerts
RECALL RECORD — CLASS IRecall closedF-1060-2019/FDA enforcement
Ottogi America INC·Food·Jan 15, 2019

Ottogi Ramen Bokki (Cup) 4.23oz X 12ea Item #21309009 Manufactured by: Ottogi Ramyon Co

What you need to know

Class I

  • What happened

    Undeclared allergen; egg.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDACA, WA, UT, IL +8 moreMore food

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Share via WhatsApp

Match before you discard

Product identification

Source: FDA FOOD

Brand nameOttogi America INC
Recalling firmOttogi America INCGardena, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • BEST BEFORE JAN.15.2019 to BEST BEFORE NOV.21.2019
Distribution area
CAWAUTILTXNJGANVCOHIORAZ

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

United States, Canada

Quantity affected1, 594, 338 units
Recall initiationFDA report date: March 6, 2019
FDA recall numberF-1060-2019

Beyond the headline

The recall, in context

Ottogi America INC initiated this food recall on January 15, 2019. The FDA enforcement report states: Undeclared allergen; egg. The FDA report lists distribution as: U.S. distribution to the following: CA, WA, UT, IL, TX, NJ, GA, NV, CO, HI, OR, AZ Foreign distribution to the following: Canada.

The FDA enforcement report describes the reason as: Undeclared allergen; egg.

Ottogi Ramen Bokki (Cup) 4.23oz X 12ea Item #21309009 Manufactured by: Ottogi Ramyon Co was made or distributed by Ottogi America INC in Gardena, CA, United States. This page reflects FDA report F-1060-2019, dated March 6, 2019.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared egg

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with an egg allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed egg allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have an egg allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Ottogi Ramen Bokki (Cup) 4.23oz X 12ea Item #21309009 Manufactured by: Ottogi Ramyon Co recall?

Ottogi America INC recalled Ottogi Ramen Bokki (Cup) 4.23oz X 12ea Item #21309009 Manufactured by: Ottogi Ramyon Co in an FDA Class I enforcement action reported as F-1060-2019. Undeclared allergen; egg.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have an egg allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Ottogi America INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1060-2019. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Ottogi America INC

View brand
Class I·

Ottogi America INC

Ottogi Spicy Seafood Flavor Udon Odongtong 5pk 1lb 5.16oz X 8pk Item #32142410 Manufactured by: …

Undeclared allergen; egg.

CA, WA, UT +9 more +1 countriesFood
Class I·

Ottogi America INC

Ottogi Ramen Sari (Extra Noodle) 3.88oz X 48ea Item #21101009 Manufactured by: Ottogi Ramyon Co

Undeclared allergen; egg.

CA, WA, UT +9 more +1 countriesFood

Related alerts

Recent Undeclared allergens recalls

All alerts
Class I·

Oliva on Main

Riad's Oliva to Go Spicy Baba Ghanouj

Contains undeclared sesame

MA, CTFood
Class I·

Oliva on Main

Riad's Oliva to Go Baba Ghanouj

Contains undeclared sesame

MA, CTFood

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.