---
title: "Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film W... — FDA record H-1186-2026 | Is It on Recall"
description: "Undeclared Allergen (Fish)"
url: https://isitonrecall.com/recall/fda-food-h-1186-2026-fusia-asian-inspirations-kimchi-tofu-kimbap-8-1-oz-230-g-paper-film-wrapper-12-packages-per-case-6-e/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea: Kim... — FDA record H-1186-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 25, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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 .
- **Reason**: Undeclared Allergen (Fish)
- **Classification**: Class I
- **Recalling firm**: GELLERT GLOBAL GROUP
- **Quantity**: 29,850 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: H-1186-2026

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1186-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Best if Used By: October 8, 2027 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Connecticut](https://isitonrecall.com/state/connecticut/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)

## Dates in the source

- **Report date**: Jul 29, 2026
- **Recall initiation date**: Jun 25, 2026
- **Center classification date**: Jul 23, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1186-2026%22)

## Related records

[Tuna records](https://isitonrecall.com/product/tuna/) [Seafood records](https://isitonrecall.com/category/seafood/) [GELLERT GLOBAL GROUP records](https://isitonrecall.com/brand/gellert-global-group/)