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RECALL RECORD — CLASS IRecall closedF-0803-2018/FDA enforcement
J F C International INC·Food·Feb 1, 2018

Daisho Kimchi Hot Pot Soup Base

What you need to know

Class I

  • What happened

    Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Fish-derived ingredients were omitted from the label, creating a risk for fish-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, NV, WA, OR +24 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameJ F C International INC
Recalling firmJ F C International INCCommerce, CA, United States
UPC / barcodes
4 904621 04221 9
Lot / date codes
  • All lots
Distribution area
CANVWAORUTAKAZTXOKOHMOKYMIWINEILINKSNYCTNJPAMAMDDEDCVAHI

CA, NV, WA, OR, UT, AK, AZ, TX, OK, OH, MO, KY, MI, WI, NE, IL. IN, KS, NY, CT, NJ, PA, MA, MD, DE, DC, VA, HI.

United States

Quantity affected2563 cases and 3 pouches
Recall initiationFDA report date: February 14, 2018
FDA recall numberF-0803-2018

Beyond the headline

The recall, in context

J F C International INC initiated this food recall on February 1, 2018. The FDA enforcement report states: Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab. The FDA report lists distribution as: CA, NV, WA, OR, UT, AK, AZ, TX, OK, OH, MO, KY, MI, WI, NE, IL. IN, KS, NY, CT, NJ, PA, MA, MD, DE, DC, VA, HI.

The FDA enforcement report describes the reason as: Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.

Daisho Kimchi Hot Pot Soup Base was made or distributed by J F C International INC in Commerce, CA, United States. This page reflects FDA report F-0803-2018, dated February 14, 2018.

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 UPC and lot code 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 fish

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish 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 fish allergy, especially anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a fish 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 Daisho Kimchi Hot Pot Soup Base recall?

J F C International INC recalled Daisho Kimchi Hot Pot Soup Base in an FDA Class I enforcement action reported as F-0803-2018. Daisho Kimchi Hot Pot Soup base contains undeclared fish - shrimp and crab.

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 a fish 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 J F C International 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-0803-2018. 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

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