RecallHawk
Class II Recall

Chin Jung White Kimchi - 3 lb. 8 oz (1.58 kg) plastic jars

Chin Jung Corporation

Summary

The FDA issued a Class II for Chin Jung White Kimchi - 3 lb. 8 oz (1.58 kg) plastic jars by Chin Jung Corporation. Reason: Undeclared allergen; fish.

Details

Source

Food Recall

External ID

F-0931-2024

Action Date

2024-03-06

Status

Terminated

Category

food

Product Description

Chin Jung White Kimchi - 3 lb. 8 oz (1.58 kg) plastic jars

Lot/Code Info: Firm does not apply lot codes or expiration dates to jars

Quantity Affected: 1,274 jars

Reason for Recall

Undeclared allergen; fish

Distribution

U.S. distribution to customers (supermarkets) in California, Colorado, Nevada.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-02-16

Company

Chin Jung Corporation

Los Angeles, CA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 128 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Chin Jung Corporation has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Chin Jung Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Chin Jung Corporation have FDA actions?

Chin Jung Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0931-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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