Kashk (Whey) Ingredients: Whey, Water, Salt Nader Trading Inc., 1821 E. Dryer Road, Santa Ana, CA 92705 UPC# 68535700153
Summary
The FDA issued a Class II for Kashk (Whey) Ingredients: Whey, Water, Salt Nader Trading Inc., 1821 E. Dryer Ro by Nader Trading, Inc.. Reason: Finished product label fails to include Milk in ingredient listing. (Undeclared Allergen).
Details
Source
Food Recall
External ID
F-0674-2025
Action Date
2025-04-09
Status
Terminated
Category
food
Product Description
Kashk (Whey) Ingredients: Whey, Water, Salt Nader Trading Inc., 1821 E. Dryer Road, Santa Ana, CA 92705 UPC# 685357001537
Lot/Code Info: Lot# 15412645 Expiration date: 01/21/2026
Quantity Affected: 1008 jars
Reason for Recall
Finished product label fails to include Milk in ingredient listing. (Undeclared Allergen)
Distribution
MD, VA, and CA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-25
Company
Santa Ana, 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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Nader 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 Nader Trading, Inc. have FDA actions?
This is the only FDA action we have on record for Nader Trading, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0674-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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