RecallRadar
ModerateReported May 20, 2026 (6 weeks ago)

...And Kimchi branded kimchi

Recalled by Ocinet, Inc.

Food recall

Ocinet, Inc.

Class II — moderate

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

See all recalls involving an undeclared allergen

Ocinet, Inc. has recalled ...And Kimchi branded kimchi, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 20, 2026 and was initiated on May 1, 2026. 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 ...And Kimchi branded kimchi, with approximately 199,750 units (across 3 different sizes) affected. The company behind the recall is Ocinet, Inc., based in Downey, CA. The FDA describes the product as: “...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411”

Why was ...And Kimchi branded kimchi recalled?

According to the FDA, the stated reason for the recall is: “Undeclared allergen ingredient (fish).” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought ...And Kimchi branded kimchi, compare it against the product description and identifying codes (No lot numbers provided. Recall includes all product.) 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 Ocinet, 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
May 20, 2026
Recall started
May 1, 2026
Distributed in
CA
What was recalled
...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411
Why it was recalled (as stated by the FDA)
Undeclared allergen ingredient (fish)
How to identify the affected product
No lot numbers provided. Recall includes all product.
Amount recalled
199,750 units (across 3 different sizes)

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 ...And Kimchi branded kimchi recalled?+

According to the FDA: Undeclared allergen ingredient (fish)

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 ...And Kimchi branded kimchi?+

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-0780-2026. Information last synced from the FDA on July 6, 2026.