RecallHawk
Class I Recall

Chois Kimchi Company Gluten Free Gochujang Red Chili Paste, packaged 16oz plastic pouch with spout, keep refrigerated. U

Choi's Kimchi LLC

Summary

The FDA issued a Class I for Chois Kimchi Company Gluten Free Gochujang Red Chili Paste, packaged 16oz plasti by Choi's Kimchi LLC. Reason: Salmonella..

Details

Source

Food Recall

External ID

F-0055-2025

Action Date

2024-10-30

Status

Terminated

Category

food

Product Description

Chois Kimchi Company Gluten Free Gochujang Red Chili Paste, packaged 16oz plastic pouch with spout, keep refrigerated. UP 8 58878 00330 8. Made By Chois Kimchi, LLC Portland, OR 97230.

Lot/Code Info: LOT CODE: 081525. Best By: 08/15/25.

Quantity Affected: 11 cases (6 pouches per case)

Reason for Recall

Salmonella.

Distribution

Distributed in Oregon and Washington.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-10-03

Company

Choi's Kimchi LLC

Portland, OR

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 42 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Choi's Kimchi LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Choi's Kimchi LLC have FDA actions?

This is the only FDA action we have on record for Choi's Kimchi LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0055-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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