PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK TRADING INC.; INGREDIENTS: Kumquat slices; packaged in clear
Summary
The FDA issued a Class II for PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK TRADING INC.; INGRED by East CK Trading Inc.. Reason: Product contains undeclared sulfites (7.49mg/serving).
Details
Source
Food Recall
External ID
F-0778-2025
Action Date
2025-05-21
Status
Terminated
Category
food
Product Description
PRESIDENT BRAND; Kumquat Slices; NET WT. 8 OZ/227g; EAST CK TRADING INC.; INGREDIENTS: Kumquat slices; packaged in clear plastic jars with UPC 8 10077 20936 3
Lot/Code Info: No additional coding.
Quantity Affected: 775 bottles +
Reason for Recall
Product contains undeclared sulfites (7.49mg/serving)
Distribution
NY, TX, NJ, MD
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-23
Company
Long Island City, NY
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 51 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 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 (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-0778-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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