RecallRadar
FDA · FoodClass I

Gellert Global Group food recall: Fusia

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
99357
Recall initiated
Jun 25, 2026
Classified by FDA
Jul 23, 2026
Posted in Enforcement Report
Jul 29, 2026
Recalling firm
GELLERT GLOBAL GROUP
Firm location
Elizabeth, NJ, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Undeclared Allergen (Fish)

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Jun 25, 2026. FDA classified it 28 days later, on Jul 23, 2026. Distribution reported by FDA: The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD GELLERT GLOBAL GROUP has 2 recalls in our records.

Recalled products (1)

  • H-1186-2026 Class I Ongoing

    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 .

    Codes / lots: Best if Used By: October 8, 2027

    Quantity: 29,850 units

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 99357
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.