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Ended FDAEvent 99357 (3 months ago)

Fusia Asian Inspirations Kimbap

Fusia Asian Inspirations Kimchi & Tofu Kimbap may contain undeclared fish, posing a risk of serious allergic reaction.

Recall ended Sep 22, 2026. Still check yours.

High risk

There is a reasonable chance that eating it could cause serious health problems or death.

FDA Class I recall · How risk is rated

2 photos

What to do

What happened

Gellert Global Group of Elizabeth, New Jersey, recalled 8.1 oz packages of ALDI Brand Fusia Asian Inspirations Kimchi & Tofu Kimbap because they may contain undeclared fish (tuna). People with an allergy or severe sensitivity to fish risk a serious or life-threatening allergic reaction. The recall began June 25, 2026, and was announced July 2, 2026.

The product, packaged in a paper film wrapper with 12 packages per case, was distributed to New York, Pennsylvania, Connecticut, North Carolina, Texas, and Maryland. The affected items include 6 Kimchi & Tofu Kimbap and 6 Spicy Tuna with Gochujang Kimbap per case, Keep Frozen-Do Not Thaw.

Summary by Recall Canary from the FDA notice.

What to do

If a code on your package matches:

  1. Consumers who have purchased the 8.1 oz packages of ALDI Brand Fusia Asian Inspirations Kimchi & Tofu Kimbap are urged to return it to the place of purchase for a full refund.
  2. Consumers with questions may contact the company at 1-908-351-8000 Monday-Friday 8:30 am-5:00 pm EST. Email fsqaincidents@gellertglobalgroup.com.

Is yours affected?

Affected if its best-by date matches.

  1. Fusia Asian Inspirations Kimchi & Tofu Kimbap

    Best-by
    OCT.08.2027

Details

Company began the recall
Sold in

The adulterated product was distributed to the following states: New York, Pennsylvania, Connecticut, North Carolina, Texas, Maryland

Event ID
99357
Recall No.
H-1186-2026
Company
GELLERT GLOBAL GROUPElizabeth, New Jersey
Quantity recalled
29,850 units
Recall type
Voluntary: Firm initiated
Customers told by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
  1. Company began the recall

  2. Announced by the company

  3. Listed on Recall Canary

  4. Added to FDA's Enforcement Report · Classified by FDA

  5. In FDA's weekly enforcement report

  6. Recall ended

  7. Summary updated

All recalls from GELLERT GLOBAL GROUP

Summary by Recall Canary, written with AI · summary updated Oct 12, 2026 · primary source: U.S. Food and Drug Administration