RecallRadar
FDA · FoodClass I

JJWV Marketing Corporation food recall: Ankimo branded Monkfish Liver

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
96757
Recall initiated
Apr 21, 2025
Classified by FDA
May 7, 2025
Posted in Enforcement Report
May 14, 2025
Terminated
Aug 7, 2026
Recalling firm
JJWV Marketing Corporation
Firm location
Santa Fe Springs, CA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
E-Mail
Products in this event
1

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.

View the official FDA record ↗

Reason for recall

Undeclared allergen ingredient (milk)

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 Apr 21, 2025. FDA classified it 16 days later, on May 7, 2025. Distribution reported by FDA: see attached distribution document. All California direct consignees. Have not determine if product was distributed out of state.

Recalled products (1)

  • F-0761-2025 Class I Terminated

    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

    Codes / lots: best by date: 20271017

    Quantity: 346 cases from lot 2026 and 0 cases from lot 2027

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 96757
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.