Belevini BICHKI, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK,20 PACKAGES PER CASE, FROZEN, REFR
Summary
The FDA issued a Class I for Belevini BICHKI, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM by MAMTAKIM, Inc.. Reason: Clostridium botulinum (uneviscerated fish).
Details
Source
Food Recall
External ID
H-0312-2026
Action Date
2025-12-24
Status
Terminated
Category
food
Product Description
Belevini BICHKI, Dried Salted Whole Smelts, Net. Weight, 5.29 oz (150 g) VACUUM PACK,20 PACKAGES PER CASE, FROZEN, REFRIGERATE AFTER OPENING
Lot/Code Info: PRODUCT NUMBER: LL0321, BAR CODE: 0754684899008
Quantity Affected: 4 Cases
Reason for Recall
Clostridium botulinum (uneviscerated fish)
Distribution
The adulterated product was distributed to the following states: NY, TX, PA, NJ, FL.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-27
Company
Elizabeth, NJ
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 87 food recalls issued in the same week, part of 204 food-related FDA actions this month.
MAMTAKIM, Inc. has 4 FDA actions in our database, including 4 recalls.
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 (MAMTAKIM, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does MAMTAKIM, Inc. have FDA actions?
MAMTAKIM, Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0312-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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