Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen
Summary
The FDA issued a Class I for Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep f by EURO FOODS GROUP USA NJ INC. Reason: The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying..
Details
Source
Food Recall
External ID
H-1331-2026
Action Date
2026-09-16
Status
Ongoing
Category
food
Product Description
Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen
Lot/Code Info: BATCH NO: 130 EF, 146 EF SERIAL NUMBER: 5055192640140 PRODUCT CODE: 28DSUM
Quantity Affected: 53 boxes
Reason for Recall
The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.
Distribution
The adulterated product was distributed to the following states: VA, NY, NJ, MI
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-01
Company
Totowa, NJ
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 24 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (EURO FOODS GROUP USA NJ INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does EURO FOODS GROUP USA NJ INC have FDA actions?
This is the only FDA action we have on record for EURO FOODS GROUP USA NJ INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1331-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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