CLASS I ONGOING Food recall · Reported 29 Jul 2026 · FDA Enforcement Report

Fusia, Asian Inspirations, Kimchi & Tofu Kimbap , 6 ea recalled

Gellert Global Group is recalling Fusia, Asian Inspirations, Kimchi & Tofu Kimbap , 6 ea: Kimchi & Tofu Kimbap / 6 ea Spicy, distributed in Connecticut, Maryland, North Carolina, New York, Pennsylvania, Texas. The recall was initiated on 25 Jun 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest if Used By: October 8, 2027
Quantity recalled29,850 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-1186-2026
FDA event ID
99357
Recalling firm
Gellert Global Group, Elizabeth, NJ
Brand
Fusia
Classification
Class I
Status
Ongoing
Recall initiated
25 Jun 2026
FDA classified
23 Jul 2026
Reported
29 Jul 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Allergens
Product category
Plant-Based Meat

Timeline

25 Jun 2026Recall initiated by company
23 Jul 2026Classified by FDA+28 days
29 Jul 2026Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared Allergen (Fish)

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

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 .

Where it was distributed

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

ConnecticutMarylandNorth CarolinaNew YorkPennsylvaniaTexas

Questions about this recall

Why was it recalled?

Undeclared Allergen (Fish)

Which lots are affected?

Best if Used By: October 8, 2027

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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