CLASS I ONGOING Food recall · Reported 16 Sep 2026 · FDA Enforcement Report

Crown Farms Dried Suri Cut, 200 gm per, keep frozen recalled

Euro Foods Group USA NJ is recalling Crown Farms Dried Suri Cut, 200 gm per, keep frozen, distributed in Michigan, New Jersey, New York, Virginia. The recall was initiated on 1 Aug 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBATCH NO: 130 EF, 146 EF SERIAL NUMBER: 5055192640140 PRODUCT CODE: 28DSUM
Quantity recalled53 boxes

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-1331-2026
FDA event ID
99684
Recalling firm
Euro Foods Group USA NJ, Totowa, NJ
Brand
Crown
Classification
Class I
Status
Ongoing
Recall initiated
1 Aug 2026
FDA classified
4 Sep 2026
Reported
16 Sep 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Foreign Material
Product category
Other

Timeline

1 Aug 2026Recall initiated by company
4 Sep 2026Classified by FDA+34 days
16 Sep 2026Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen

Where it was distributed

The adulterated product was distributed to the following states: VA, NY, NJ, MI

MichiganNew JerseyNew YorkVirginia

Questions about this recall

Why was it recalled?

The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.

Which lots are affected?

BATCH NO: 130 EF, 146 EF SERIAL NUMBER: 5055192640140 PRODUCT CODE: 28DSUM

Where was it sold?

The adulterated product was distributed to the following states: VA, NY, NJ, MI

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 22 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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