...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz U
Summary
The FDA issued a Class II for ...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63 by Ocinet, Inc.. Reason: Undeclared allergen ingredient (fish).
Details
Source
Food Recall
External ID
H-0780-2026
Action Date
2026-05-20
Status
Ongoing
Category
food
Product Description
...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411
Lot/Code Info: No lot numbers provided. Recall includes all product.
Quantity Affected: 199,750 units (across 3 different sizes)
Reason for Recall
Undeclared allergen ingredient (fish)
Distribution
Product was distributed to locations in California, Texas and Georgia.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-01
Company
Downey, 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 97 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Ocinet, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ocinet, Inc. have FDA actions?
This is the only FDA action we have on record for Ocinet, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0780-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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