The Recall Desk
ModerateFDA (Food)·F-0868-2023·Announced 2023-05-17

Daisho Kimchi Hotpot Soup Recalled for Incomplete Allergen Labeling

Daisho Kimchi hotpot soup is recalled due to incomplete allergen labeling. The label warns for fish but does not specify anchovy or sardine, and the Canadian product lists clams in ingredients but not in the allergen statement.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: This is an FDA Class III recall with no reported illnesses or injuries. The hazard is incomplete and inconsistent allergen labeling that could affect consumers with fish or shellfish allergies. As a labeling defect without confirmed harm, it represents a theoretical risk rather than an imminent health threat.

Plain-English summary

Daisho Kimchi hotpot soup (750g, UPC 4904621042653) is being recalled by the FDA due to allergen labeling discrepancies. The product label warns for fish but does not specify which fish ingredients are present, such as anchovy or sardine. In the Canadian version, clams are listed in the ingredient list but are not identified in the allergen contains statement.

Approximately 4,078 units were distributed to retail locations across California, Texas, Nevada, New York, New Jersey, Washington, and British Columbia, Canada.

Consumers with allergies or sensitivities to fish, anchovy, sardine, or clams may be affected by this labeling error.

The recalled product

Product
Daisho Kimchi hotpot soup 750g UPC: 4904621042653
Affected units
4,078

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • No code on package

Distribution

Distributed in 6 states:

Part of a larger recall action

This product is one of 21 recalled by DAISO CALIFORNIA WAREHOUSE under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 21 products in this recall →