Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported and DIST. BY: JJWV Marketing Corporation; Santa Fe Springs,
Summary
The FDA issued a Class I for Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported and DIST. BY: JJWV by JJWV Marketing Corporation. Reason: Undeclared allergen ingredient (milk).
Details
Source
Food Recall
External ID
F-0761-2025
Action Date
2025-05-14
Status
Completed
Category
food
Product Description
Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported and DIST. BY: JJWV Marketing Corporation; Santa Fe Springs, CA 90670 USA; UPC# 8 94042 00256 2
Lot/Code Info: best by date: 20271017
Quantity Affected: 346 cases from lot 2026 and 0 cases from lot 2027
Reason for Recall
Undeclared allergen ingredient (milk)
Distribution
see attached distribution document. All California direct consignees. Have not determine if product was distributed out of state.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-21
Company
Santa Fe Springs, CA
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 22 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 (JJWV Marketing Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does JJWV Marketing Corporation have FDA actions?
This is the only FDA action we have on record for JJWV Marketing Corporation in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0761-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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