RecallRadar
ModerateReported December 31, 2025

Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantit…

Recalled by Karabetian Import and Distribution, Inc.

Food recall

Karabetian Import and Distribution, Inc.

Class II — moderate

Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Karabetian Import and Distribution, Inc. has recalled Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantit…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 31, 2025 and was initiated on November 18, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantit…, with approximately 338 boxes across all recalled products affected. The company behind the recall is Karabetian Import and Distribution, Inc., based in Los Angeles, CA. The FDA describes the product as: “Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantity per case: 380 g paper carton/tray - 9/case UPC: 5201592015822”

Why was Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantit… recalled?

According to the FDA, the stated reason for the recall is: “partially hydrogenated oils (PHOs) in foods exported to the US.”

What should you do?

If you think you may have bought Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantit…, compare it against the product description and identifying codes (Lot: 048025 Exp date 02/17/2026 Lot: 122025 Exp date: 11/02/2026 Lot:248025 Exp date: 05/09/2027) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Karabetian Import and Distribution, Inc. or your local health authority.

About this recall

This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Ongoing
Date reported
December 31, 2025
Recall started
November 18, 2025
Distributed in
CA
What was recalled
Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantity per case: 380 g paper carton/tray - 9/case UPC: 5201592015822
Why it was recalled (as stated by the FDA)
partially hydrogenated oils (PHOs) in foods exported to the US
How to identify the affected product
Lot: 048025 Exp date 02/17/2026 Lot: 122025 Exp date: 11/02/2026 Lot:248025 Exp date: 05/09/2027
Amount recalled
338 boxes across all recalled products

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantit… recalled?+

According to the FDA: partially hydrogenated oils (PHOs) in foods exported to the US

How serious is this recall?+

Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

What should I do if I have Product: Zimi Kunefe Ready to eat (Frozen) Package Size and quantit…?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0332-2026. Information last synced from the FDA on July 6, 2026.

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