Class IITerminatedVoluntary: Firm initiated
Ocinet, Inc.: food recall H-0780-2026
Ocinet, Inc. of Downey, CA recalled ...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz… Reason: Undeclared allergen ingredient (fish). The FDA listed it as Class II in its Enforcement Report dated May 20, 2026; distribution: California, Georgia, Texas.
Record status as published: Terminated (terminated Aug 4, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- ...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411
- Product quantity
- 199,750 units (across 3 different sizes)
- Reason for recall
- Undeclared allergen ingredient (fish)
- Codes, lots and dates on the package
- No lot numbers provided. Recall includes all product.
- Distribution pattern
- Product was distributed to locations in California, Texas and Georgia.
- Recalling firm
- Ocinet, Inc., Downey, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Telephone
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 1, 2026 |
| Classified by the FDA | May 14, 2026 |
| Published in the Enforcement Report | May 20, 2026 |
| Terminated | Aug 4, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0780-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.