Class IFood recall: undeclared fish
Fusia, Asian Inspirations, Kimchi & Tofu Kimbap
GELLERT GLOBAL GROUP, of Elizabeth, NJ, began recalling this product on . FDA classified the recall as Class I on .
Why it was recalled
In FDA’s words:
Undeclared Allergen (Fish)
The allergen tags on this page are ours, matched from FDA’s words above.
The product
Fusia, Asian Inspirations, Kimchi & Tofu Kimbap
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 .
- Codes and dates
- Best if Used By: October 8, 2027
- Quantity
- 29,850 units
- Recall number
- H-1186-2026
Where it was distributed
In FDA’s words:
The adulterated product was distributed to the following states: NY, PA, CT, NC, TX, MD
What Class I means
In FDA’s definitions, a Class I recall is one where: there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. FDA’s recall definitions
If you have this product
- FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
- FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
- If someone has a serious allergic reaction, call 911. Signs of a serious reaction
Source
FDA’s Enforcement Report, read through openFDA. This recall first appeared in the report of . openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.