Class IOngoingVoluntary: Firm initiated
GELLERT GLOBAL GROUP: food recall H-1186-2026
GELLERT GLOBAL GROUP of Elizabeth, NJ recalled Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea:… Reason: Undeclared Allergen (Fish). The FDA listed it as Class I in its Enforcement Report dated Jul 29, 2026; distribution: Connecticut, Maryland, North Carolina, New York, Pennsylvania, Texas.
Record status as published: Ongoing. 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
- Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea: Kimchi & Tofu Kimbap / 6 ea Spicy Tuna with Gochujang Kimbap, Keep Frozen-Do Not Thaw .
- Product quantity
- 29,850 units
- Reason for recall
- Undeclared Allergen (Fish)
- Codes, lots and dates on the package
- Best if Used By: October 8, 2027
- Distribution pattern
- The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD
- Recalling firm
- GELLERT GLOBAL GROUP, Elizabeth, NJ
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jun 25, 2026 |
| Classified by the FDA | Jul 23, 2026 |
| Published in the Enforcement Report | Jul 29, 2026 |
Other recalls by GELLERT GLOBAL GROUP
- H-1176-2026 · Jul 22, 2026 · Class II — Foreign material (Glass) was found in the product.
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-1186-2026 (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.