CLASS I Food recall · Reported 14 May 2025 · FDA Enforcement Report
Ankimo branded Monkfish Liver recalled by JJWV Marketing
JJWV Marketing is recalling Ankimo branded Monkfish Liver, distributed in California. The recall was initiated on 21 Apr 2025 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0761-2025
- FDA event ID
- 96757
- Recalling firm
- JJWV Marketing, Santa Fe Springs, CA
- Brand
- Ankimo
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Apr 2025
- FDA classified
- 7 May 2025
- Reported
- 14 May 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Allergens
- Product category
- Other
Timeline
| 21 Apr 2025 | Recall initiated by company | |
| 7 May 2025 | Classified by FDA | +16 days |
| 14 May 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared allergen ingredient (milk)
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
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
Where it was distributed
see attached distribution document. All California direct consignees. Have not determine if product was distributed out of state.
Questions about this recall
Why was it recalled?
Undeclared allergen ingredient (milk)
Which lots are affected?
best by date: 20271017
Where was it sold?
see attached distribution document. All California direct consignees. Have not determine if product was distributed out of state.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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