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Food recall · FDA · Published February 1, 2018

J F C International Inc recalls Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported

J F C International recalls Daisho Kimchi Hot Pot Soup Base pouches due to undeclared shrimp and crab. Consumers should check bar code 49 04621 04221 9 for affected products.

🇺🇸 FDA recall #F-0803-2018FoodDaisho ›
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Contact the company & request your remedy

Recalling firmJ F C International Inc7101 E Slauson Ave, N/A · Commerce, CA 90040-3622
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

J F C International has recalled Daisho Kimchi Hot Pot Soup Base pouches because they contain undeclared shrimp and crab. This could cause allergic reactions for people sensitive to shellfish. Read more at govinfonow.com/recall/19716-daisho-kimchi-hot-pot-soup-base-recall-undeclared-shrimp-and.

Source Summary by GovInfoNow · govinfonow.com/recall/19716-daisho-kimchi-hot-pot-soup-base-recall-undeclared-shrimp-and · Updated October 7, 2026 · FDA enforcement record: FDA #F-0803-2018

Cite this page

“Daisho Kimchi Hot Pot Soup Base Recall: Undeclared Shrimp and Crab.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19716-daisho-kimchi-hot-pot-soup-base-recall-undeclared-shrimp-and. Based on FDA recall #F-0803-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0803-2018%22&limit=1).

Why it’s dangerous

The soup base contains shrimp and crab without being listed on the label. This poses a risk for people with shellfish allergies who might react to these ingredients.

Who’s affected

People who have purchased the Daisho Kimchi Hot Pot Soup Base pouches (1.60 lb, 10 per case) with bar code 49 04621 04221 9 are affected. Those with shellfish allergies are at higher risk.

How to tell if you have this one

Check for the bar code 49 04621 04221 9 on the pouch. The product is a 1.60 lb pouch sold in cases of 10 units.

  • Brand
    Daisho
  • Product
    Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the bar code 49 04621 04221 9 on the pouch to confirm if it's affected.

✎ GovInfoNow

Questions people ask

Is this product safe for people without shellfish allergies?

Yes, the product is safe for people without shellfish allergies as the undeclared shrimp and crab only pose a risk for those with shellfish allergies.

How can I check if I have the recalled product?

Check the bar code 49 04621 04221 9 on the pouch. The product is a 1.60 lb pouch sold in cases of 10 units.

What should I do if I have the recalled product?

The recall does not require immediate action; check the product details to confirm if it's affected.

Take action

Contact Daisho

We’ve drafted a message you can send Daisho to request your refund or repair — edit it as you like.

Subject: Recall F-0803-2018 — Daisho Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 

Hello,

I own a Daisho Kimchi Hot Pot Soup Base; 1.60 lb pouch (10 units per case) Bar Code: 49 04621 04221 9 Product of Japan Imported that is covered by recall F-0803-2018 from Daisho.

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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Where this comes from

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.

  • Official source: FDA Recall #F-0803-2018 (February 1, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0803-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA