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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
Imported Monkfish Liver undeclared allergen (Milk)
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite side contains English label that reads: #61122; ANKIMOBO (prepared Monkfish Liver) Ingredients: Monkfish Liver, Brewed Alcohol, (Rice, Rice Malt), Enzyme. CONTAINS: Fish (Monkfish), UPC code: 72546611224 Imported By Mutual Trading Co., Inc.; El Monte, CA 91731 North American Food Dist., Co., Inc.; W. Sacramento, CA 95691; Product of China; NET WT: 7.05 OZ (200 g) "Keep Under Refrigeration"; #16143N | Not published in this source record | 70 cases | Two lots: Best By 11/15/2024 Best BY 06/30/2025 |
Responsible company: Mutual Trading Company Inc.
FDA Recall United States TerminatedTerminated: September 10, 2024Historical recordClass I
FDA Recall United States TerminatedTerminated: September 10, 2024Historical recordClass I
FDA Recall United States TerminatedTerminated: September 10, 2024Historical recordClass I
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Massachusetts | 1 |
| Maryland | 1 |
| New Jersey | 1 |
| New York | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
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.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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.
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