FDAClass I · Food · Recall H-1186-2026 · Recalled July 29, 2026

Fusia recall — GELLERT GLOBAL GROUP

Agency report date: July 29, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Fusia
Company / brand: GELLERT GLOBAL GROUP
Lot / serial / date codes: Best if Used By: October 8, 2027
Distribution: The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD

Agency product description and boundaries

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 .

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Undeclared Allergen (Fish)

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Fusia

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1186-2026
Brand: GELLERT GLOBAL GROUP
Classification: Class I
Units affected: 29,850 units
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Fusia

Companies & origin

Recalling firm location: Elizabeth, NJ, United States
Firm address: 1 Atalanta Plz, N/A, 07206

Identifying details (verbatim from the notice)

Product codes / lots: Best if Used By: October 8, 2027
Distribution: The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD
Firm notified the public via: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID: 99357
Recall initiated: June 25, 2026
FDA classified: July 23, 2026
FDA report date: July 29, 2026

Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

Report a data error on this page