ARAL FISH; ARAL SILVER VOBLA; WHOLE DRIED, SALTED ROACH FISH EVISCERATED; FISH ROE DRIED; Ingredients: whole eviscerated
Summary
The FDA issued a Class I for ARAL FISH; ARAL SILVER VOBLA; WHOLE DRIED, SALTED ROACH FISH EVISCERATED; FISH R by Krasnyi Oktyabr USA Inc. Reason: Clostridium botulinum (uneviscerated fish).
Details
Source
Food Recall
External ID
H-0391-2025
Action Date
2025-08-13
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: No Codes
Quantity Affected: 23 boxes
Reason for Recall
Clostridium botulinum (uneviscerated fish)
Distribution
AZ, CA, CO, FL, GA, KS, MA, MI, MN, MO, NY, OH, PA, TX, WA, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-18
Company
Brooklyn, NY
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 108 food recalls issued in the same week, part of 204 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 (Krasnyi Oktyabr USA Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Krasnyi Oktyabr USA Inc have FDA actions?
This is the only FDA action we have on record for Krasnyi Oktyabr USA Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0391-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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