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FDA recall, , Moderate risk

...And Kimchi Branded Kimchi

Kimchi contains undeclared fish, posing a risk of serious allergic reaction.

Recall ended Aug 4, 2026. Still check yours.

What happened

Ocinet, Inc., of Downey, California, is recalling all ...And Kimchi branded sliced kimchi because the product contains undeclared fish (anchovies). The recall covers 199,750 units across three sizes of glass containers: 126oz, 63oz, and 30oz. People who have an allergy or severe sensitivity to fish run the risk of a serious o.

The company began the recall on May 1, 2026, and announced it on May 4, 2026. The product was distributed to locations in California, Texas, and Georgia.

2 photos

What to do

If a code on your package is listed below:

  1. Consumers who have purchased this Product and have concerns about the inclusion of the allergen are welcome to return the Product to the retail store where any such Product was purchased for a full refund.
  2. Consumers with questions may contact the retail store where the product was purchased as set forth below.
  3. Zion Market - San Diego, CA, (858) 268-3300.
  4. Zion Market - Irvine, CA, (714) 832-5600. Zion Market - Los Angeles, CA, (213) 302-3792. Zion Market - Buena Park, CA, (714) 367-5400.

Is yours affected?

Affected if its UPC is listed.

A UPC is the number printed under a barcode.

  1. ...And Kimchi branded kimchi

    UPC
    • 8541200408
    • 8651200409
    • 8541200411
    Lot code
    all product

From the FDA notice

...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz);

Recall details

Company began the recall
Company
Ocinet, Inc.Downey, California
Risk

Moderate risk

Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
98900
Recall number
H-0780-2026
Quantity recalled
199,750 units (across 3 different sizes)

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Announced by the company

  3. Listed on Recall Canary

  4. Added to FDA's Enforcement Report · Classified by FDA

  5. In FDA's weekly enforcement report

  6. Recall ended

  7. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 12, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)