EURO FOODS GROUP USA NJ INC Recall: The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.
United States
OngoingClass I
- Company
- EURO FOODS GROUP USA NJ INC
- Product
- Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 pack…
- Recall date
- August 1, 2026
- Source
- FDA
Reason for recall
The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen | Not published in this source record | 53 boxes | BATCH NO: 130 EF, 146 EF SERIAL NUMBER: 5055192640140 PRODUCT CODE: 28DSUM |
Distribution
- The adulterated product was distributed to the following states: VA
- NY
- NJ
- MI
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-1331-2026
- Event ID
- 99684
- Status
- Ongoing
- Classification
- Class I
- Company
- EURO FOODS GROUP USA NJ INC
- Product description
- Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen
- Quantity
- 53 boxes
- Reason
- The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.
- Recall initiation date
- August 1, 2026
- Report date
- September 16, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- The adulterated product was distributed to the following states: VA, NY, NJ, MI
- UPC, lot, and code information
- BATCH NO: 130 EF, 146 EF SERIAL NUMBER: 5055192640140 PRODUCT CODE: 28DSUM
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: EURO FOODS GROUP USA NJ INC
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Virginia | 1 |
| New York | 1 |
| New Jersey | 1 |
| Michigan | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
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