Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantity per case: 380 g paper carton/tray - 9/case UPC: 520
Summary
The FDA issued a Class II for Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantity per case: 3 by Karabetian Import and Distribution, Inc.. Reason: partially hydrogenated oils (PHOs) in foods exported to the US.
Details
Source
Food Recall
External ID
H-0332-2026
Action Date
2025-12-31
Status
Ongoing
Category
food
Product Description
Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantity per case: 380 g paper carton/tray - 9/case UPC: 5201592015822
Lot/Code Info: Lot: 048025 Exp date 02/17/2026 Lot: 122025 Exp date: 11/02/2026 Lot:248025 Exp date: 05/09/2027
Quantity Affected: 338 boxes across all recalled products
Reason for Recall
partially hydrogenated oils (PHOs) in foods exported to the US
Distribution
Distributed in the following states: AZ, CA, CO, FL, GA, ND, OR, TX, WA, and WI.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-18
Company
Los Angeles, 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 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Karabetian Import and Distribution, 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 (Karabetian Import and Distribution, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Karabetian Import and Distribution, Inc. have FDA actions?
Karabetian Import and Distribution, 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 "H-0332-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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