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Lower risk Food recall · FDA · Published June 25, 2026

Gellert Global Group Kimbap Recall: Undeclared Fish Allergen Risk

Gellert Global Group recalls 12-packs of Kimbap products due to undeclared fish allergen. Consumers should check packaging for the recall and avoid products with fish.

🇺🇸 FDA recall #H-1186-2026FoodGellert Global Group ›
✎ GovInfoNow plain-language explainer

Gellert Global Group is recalling certain Kimbap products because they contain fish that wasn't listed as an allergen. This poses a risk for people with fish allergies who might unknowingly consume the product. Read more at govinfonow.com/recall/83480-gellert-global-group-kimbap-recall-undeclared-fish-allergen-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/83480-gellert-global-group-kimbap-recall-undeclared-fish-allergen-risk · Updated August 17, 2026 · Official notice: FDA #H-1186-2026

Cite this page

“Gellert Global Group Kimbap Recall: Undeclared Fish Allergen Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/83480-gellert-global-group-kimbap-recall-undeclared-fish-allergen-risk. Based on FDA recall #H-1186-2026.

The FDA announced on June 25, 2026, that Gellert Global Group is recalling Fusia and Asian Inspirations Kimchi & Tofu Kimbap due to undeclared fish allergens. The voluntary Class I recall affects approximately 29,850 units distributed in NY, PA, CT, NC, TX, and MD.

How to tell if you have it

  • Brand: Gellert Global Group
  • Product: Fusia, Asian Inspirations, Kimchi & Tofu Kimbap
  • Size: 8.1 OZ (230 g)
  • Packaging: Paper Film Wrapper, 12 packages per case, 6 ea
  • Best if Used By: October 8, 2027
  • Distribution states: NY, PA, CT, NC, TX, MD

The hazard

The product contains undeclared fish allergens, posing a risk to consumers with fish allergies. The FDA classified this as a Class I recall, indicating a high probability of serious adverse health consequences.

Context

GovInfoNow's records show Gellert Global Group has one other recall on record since May 15, 2026, specifically for foreign glass found in Ruby Artichoke Hearts on that date. Other recent recalls of similar products include Ocinet Kimchi Recall (May 1, 2026), Koi Koi Trading Fish Balls Recall (Jan. 28, 2026), and WFM Purchasing Brussel Sprouts & Kale Slaw Recall (Dec. 31, 2025).

How to tell if you have this one

Check for the product name 'Fusia, Asian Inspirations, Kimchi & Tofu Kimbap' with a 8.1 oz (230 g) paper film wrapper. The recall includes 12 packages per case, 6 items each, and the products must be kept frozen until October 8, 2027.

  • Brand
    Gellert Global Group
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the product name 'Fusia, Asian Inspirations, Kimchi & Tofu Kimbap' with a 8.1 oz (230 g) paper film wrapper.

Where it went and when

Where it was distributed

Distributed in 6 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: yesCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Connecticut, Maryland, New York, North Carolina, Pennsylvania, Texas.

Recall timeline

FDA published this recall 34 days after the firm started it.

1. Firm started the recall: Jun 25, 202612. FDA classified it Class I: Jul 23, 202623. Published in FDA’s Enforcement Report: Jul 29, 202632026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-1186-2026 (June 25, 2026)
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA