RecallHawk
Class I Recall

President Brand Licorice Plum (8 oz., 227g)

East CK Trading Inc.

Summary

The FDA issued a Class I for President Brand Licorice Plum (8 oz., 227g) by East CK Trading Inc.. Reason: Contains undeclared sulfites, undeclared FD&C Yellow 6, and unapproved color: Amaranth (E123)..

Details

Source

Food Recall

External ID

F-0812-2025

Action Date

2025-06-04

Status

Terminated

Category

food

Product Description

President Brand Licorice Plum (8 oz., 227g)

Lot/Code Info: UPC 0077-20729

Quantity Affected: unknown

Reason for Recall

Contains undeclared sulfites, undeclared FD&C Yellow 6, and unapproved color: Amaranth (E123).

Distribution

NY, VA

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-02

Company

East CK Trading Inc.

Long Island City, NY

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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.

East CK Trading Inc. has 2 FDA actions in our database, including 2 recalls.

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 (East CK Trading Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does East CK Trading Inc. have FDA actions?

East CK Trading Inc. 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-0812-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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