CLASS II Food recall · Reported 20 May 2026 · FDA Enforcement Report
And Kimchi branded kimchi recalled by Ocinet
Ocinet is recalling And Kimchi branded kimchi, distributed in California, Georgia, Texas. The recall was initiated on 1 May 2026 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0780-2026
- FDA event ID
- 98900
- Recalling firm
- Ocinet, Downey, CA
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 1 May 2026
- FDA classified
- 14 May 2026
- Reported
- 20 May 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Undeclared Allergens
- Product category
- Other
Timeline
| 1 May 2026 | Recall initiated by company | |
| 14 May 2026 | Classified by FDA | +13 days |
| 20 May 2026 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared allergen ingredient (fish)
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63oz, 30oz); 126oz UPC- 8541200408 62oz UPC- 8651200409 30oz UPC- 8541200411
Where it was distributed
Product was distributed to locations in California, Texas and Georgia.
Questions about this recall
Why was it recalled?
Undeclared allergen ingredient (fish)
Which lots are affected?
No lot numbers provided. Recall includes all product.
Where was it sold?
Product was distributed to locations in California, Texas and Georgia.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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