Skip to content
Lower risk Food recall · FDA · Published August 1, 2026

Crown Farms Dried Suri Cut: Risk of Undersized Fish in Frozen Packs

EURO FOODS GROUP USA NJ INC recalls Crown Farms Dried Suri Cut (200g) due to improper evisceration before drying, which may lead to unsafe fish consumption. Keep frozen until recalled items are returned.

🇺🇸 FDA recall #H-1331-2026FoodCrown Farms ›
✎ GovInfoNow plain-language explainer

EURO FOODS GROUP USA NJ INC has recalled Crown Farms Dried Suri Cut (200g) because the fish wasn't properly eviscerated before drying. This could lead to unsafe consumption if the product is thawed or cooked. Read more at govinfonow.com/recall/994958-crown-farms-dried-suri-cut-risk-of-undersized-fish-in.

Source Summary by GovInfoNow · govinfonow.com/recall/994958-crown-farms-dried-suri-cut-risk-of-undersized-fish-in · Updated September 23, 2026 · Official notice: FDA #H-1331-2026

Cite this page

“Crown Farms Dried Suri Cut: Risk of Undersized Fish in Frozen Packs.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/994958-crown-farms-dried-suri-cut-risk-of-undersized-fish-in. Based on FDA recall #H-1331-2026.

The FDA announced on Aug. 1, 2026, that EURO FOODS GROUP USA NJ INC is recalling Crown Farms Dried Suri Cut because the dried ribbon fish was not properly eviscerated prior to drying.

How to tell if you have it

  • Brand: Crown Farms
  • Product: Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen
  • Batch No: 130 EF, 146 EF
  • Serial Number: 5055192640140
  • Product Code: 28DSUM
  • Distribution: VA, NY, NJ, MI

The hazard

The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying. The recall is classified as Class I.

Context

GovInfoNow's records show the brand has been involved in other recent recalls of similar products, including Prime Food Processing Dried Croaker Fish Recall: Uneviscerated Fish Hazard (2026-02-03) and Recall: Prime Food Processing Dried Herring Fish due to Botulism Risk (2026-06-02). Other recent recalls of similar products include African Food on Wheels Oven Dried Fish Recall: Botulism Risk from Uneviscerated Fish (2025-11-05).

How to tell if you have this one

Check for the batch number 130 EF or 146 EF, and serial number 5055192640140 on the plastic pack. The product is sold in 25-pack boxes that must be kept frozen.

  • Brand
    Crown Farms
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for batch numbers 130 EF or 146 EF and serial number 5055192640140 on the plastic pack.

Where it went and when

Where it was distributed

Distributed in 4 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “The adulterated product was distributed to the following states: VA, NY, NJ, MI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Michigan, New Jersey, New York, Virginia.

Recall timeline

FDA published this recall 46 days after the firm started it.

1. Firm started the recall: Aug 1, 202612. FDA classified it Class I: Sep 4, 202623. Published in FDA’s Enforcement Report: Sep 16, 202634. Added to GovInfoNow: Sep 23, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest food recalls

Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-1331-2026 (August 1, 2026)
  • Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA