Fusia Asian Inspirations Kimchi & Tofu Kimbap Recall for Undeclared Fish
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Gellert Global Group recalls 29,850 units of Fusia Asian Inspirations Kimchi & Tofu Kimbap due to undeclared fish allergen.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 12, 2026 and geographically references NY, PA, CT, NC, TX, MD. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened
Gellert Global Group is recalling Fusia Asian Inspirations Kimchi & Tofu Kimbap because the product contains an undeclared fish allergen.
Which Products Are Affected
The recall involves 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. A total of 29,850 units with Best if Used By: October 8, 2027 are affected. The product was distributed to NY, PA, CT, NC, TX, MD.
What You Should Do
Consumers should not eat the product if they have a fish allergy.
Why This Matters
This is a Class I recall for an undeclared allergen that may cause serious or life-threatening allergic reactions.
Source
FDA recall H-1186-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (796 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 12, 2026.
Frequently Asked Questions
Common questions about this FDA recall.