MAMTAKIM, Inc. food recall: Belevini KORUSHKA
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97979
- Recall initiated
- Oct 27, 2025
- Classified by FDA
- Dec 16, 2025
- Posted in Enforcement Report
- Dec 24, 2025
- Terminated
- Mar 25, 2026
- Recalling firm
- MAMTAKIM, Inc.
- Firm location
- Elizabeth, NJ, 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
- 2
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.
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 Oct 27, 2025. FDA classified it 50 days later, on Dec 16, 2025. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: The adulterated product was distributed to the following states: NY, TX, PA, NJ, FL. MAMTAKIM, Inc. has 3 recalls in our records.
Recalled products (2)
H-0311-2026 Class I Terminated
Belevini KORUSHKA, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK, 20 PACKAGES PER CASE, FROZEN, REFRIGERATE AFTER OPENING
Codes / lots: PRODUCT NUMBER: LL0320, BAR CODE: 0754684898995
Quantity: 45 Cases
H-0312-2026 Class I Terminated
Belevini BICHKI, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK,20 PACKAGES PER CASE, FROZEN, REFRIGERATE AFTER OPENING
Codes / lots: PRODUCT NUMBER: LL0321, BAR CODE: 0754684899008
Quantity: 4 Cases
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 97979
- 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.