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Nader Trading, Inc. Recall: Finished product label fails to include Milk in ingredient listing. (Undeclared Allergen)

United States

TerminatedClass II

Company
Nader Trading, Inc.
Product
Kashk (Whey) Ingredients: Whey, Water, Salt Nader Trading In…
Recall date
March 25, 2025
Terminated
July 15, 2025
Source
FDA

Reason for recall

Finished product label fails to include Milk in ingredient listing. (Undeclared Allergen)

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Kashk (Whey) Ingredients: Whey, Water, Salt Nader Trading Inc., 1821 E. Dryer Road, Santa Ana, CA 92705 UPC# 685357001537 Not published in this source record 1008 jars Lot# 15412645 Expiration date: 01/21/2026

Distribution

  • MD
  • VA
  • and CA

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0674-2025
Event ID
96575
Status
Terminated
Classification
Class II
Company
Nader Trading, Inc.
Product description
Kashk (Whey) Ingredients: Whey, Water, Salt Nader Trading Inc., 1821 E. Dryer Road, Santa Ana, CA 92705 UPC# 685357001537
Quantity
1008 jars
Reason
Finished product label fails to include Milk in ingredient listing. (Undeclared Allergen)
Recall initiation date
March 25, 2025
Report date
April 9, 2025
Classification date
Not published in this source record
Termination date
July 15, 2025
Distribution pattern
MD, VA, and CA
UPC, lot, and code information
Lot# 15412645 Expiration date: 01/21/2026
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Nader Trading, Inc.

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Maryland 1
Virginia 1
California 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.