Belevini BICHKI Dried Salted Whole Smelts
Reason Clostridium botulinum (uneviscerated fish)
Belevini KORUSHKA Dried Salted Whole Smelts recall
Recalled by MAMTAKIM, Inc. · Elizabeth, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Clostridium botulinum (uneviscerated fish)
Pathogen: Botulism
Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Belevini KORUSHKA, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK, 20 PACKAGES PER CASE, FROZEN, REFRIGERATE AFTER OPENING
Quantity: 45 Cases
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
PRODUCT NUMBER: LL0320, BAR CODE: 0754684898995
Where it was sold
Florida New Jersey New York Pennsylvania Texas
FDA's distribution note: The adulterated product was distributed to the following states: NY, TX, PA, NJ, FL.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- MAMTAKIM, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 27, 2025
- In FDA report of
- Dec 24, 2025
- Terminated
- Mar 25, 2026
- FDA recall number
- H-0311-2026 · event 97979
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
Other recalls by MAMTAKIM, Inc.
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