Food Recall Check
Class I · High risk Terminated Initiated Apr 21, 2025 (1 years ago)

Ankimo branded Monkfish Liver recall

Recalled by JJWV Marketing Corporation · Santa Fe Springs, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared allergen ingredient (milk)

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

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

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.

best by date: 20271017

Where it was sold

California

FDA's distribution note: see attached distribution document. All California direct consignees. Have not determine if product was distributed out of state.

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. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. 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
JJWV Marketing Corporation
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 21, 2025
In FDA report of
May 14, 2025
Terminated
Aug 7, 2026
FDA recall number
F-0761-2025 · event 96757
Official record
FDA enforcement report search