JJWV Marketing Corporation Recall: Undeclared allergen ingredient (milk)
United States
CompletedClass I
- Company
- JJWV Marketing Corporation
- Product
- Ankimo branded Monkfish Liver; NET WT. 7 OZ (200g); Imported…
- Recall date
- April 21, 2025
- Source
- FDA
Reason for recall
Undeclared allergen ingredient (milk)
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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 | Not published in this source record | 346 cases from lot 2026 and 0 cases from lot 2027 | best by date: 20271017 |
Distribution
- see attached distribution document. All California direct consignees. Have not determine if product was distributed out of state.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0761-2025
- Event ID
- 96757
- Status
- Completed
- Classification
- Class I
- Company
- JJWV Marketing Corporation
- 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
- Quantity
- 346 cases from lot 2026 and 0 cases from lot 2027
- Reason
- Undeclared allergen ingredient (milk)
- Recall initiation date
- April 21, 2025
- Report date
- May 14, 2025
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- see attached distribution document. All California direct consignees. Have not determine if product was distributed out of state.
- UPC, lot, and code information
- best by date: 20271017
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: JJWV Marketing Corporation
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Completed." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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