CLASS I Food recall · Reported 4 Jun 2025 · FDA Enforcement Report

President Licorice Plum recalled by East CK Trading

East CK Trading is recalling President Licorice Plum, distributed in New York, Virginia. The recall was initiated on 2 May 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUPC 0077-20729
Quantity recalledunknown

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0812-2025
FDA event ID
96828
Recalling firm
East CK Trading, Long Island City, NY
Classification
Class I
Status
Terminated
Recall initiated
2 May 2025
FDA classified
23 May 2025
Reported
4 Jun 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sulfites
Product category
Candy

Timeline

2 May 2025Recall initiated by company
23 May 2025Classified by FDA+21 days
4 Jun 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

NY, VA

New YorkVirginia

Questions about this recall

Why was it recalled?

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

Which lots are affected?

UPC 0077-20729

Where was it sold?

NY, VA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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