RecallRadar
FDA · FoodClass I

Krasnyi Oktyabr USA Inc food recall: Aral Fish

Botulism risk

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
97268
Recall initiated
Jun 18, 2025
Classified by FDA
Aug 6, 2025
Posted in Enforcement Report
Aug 13, 2025
Terminated
May 21, 2026
Recalling firm
Krasnyi Oktyabr USA Inc
Firm location
Brooklyn, NY, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Clostridium botulinum (uneviscerated fish)

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Jun 18, 2025. FDA classified it 49 days later, on Aug 6, 2025. Distribution reported by FDA: AZ, CA, CO, FL, GA, KS, MA, MI, MN, MO, NY, OH, PA, TX, WA, WI Krasnyi Oktyabr USA Inc has 4 recalls in our records.

Recalled products (1)

  • H-0391-2025 Class I Terminated

    ARAL FISH; ARAL SILVER VOBLA; WHOLE DRIED, SALTED ROACH FISH EVISCERATED; FISH ROE DRIED; Ingredients: whole eviscerated dried roach fish, caviar may be present, salt.; Distributed by Krasnyi Oktyabr; PERISHABLE KEEP REFRIGERATED AT OR BELOW 40F; PRODUCT OF KAZAKHSTAN

    Codes / lots: No Codes

    Quantity: 23 boxes

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 97268
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.