Recall archive / FDA food enforcement
Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite si... — FDA record F-0534-2025
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jan 15, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- 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
- Reason
- Imported Monkfish Liver undeclared allergen (Milk)
- Classification
- Class I
- Recalling firm
- Mutual Trading Company Inc.
- Quantity
- 70 cases
- Agency-reported status
- Terminated
- Source record identifier
- F-0534-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Two lots: Best By 11/15/2024 Best BY 06/30/2025 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Firm distributed product in CT, FL, GA, MA, MD, NJ, NY
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Feb 12, 2025
- Recall initiation date
- Jan 15, 2025
- Center classification date
- Feb 6, 2025
- Termination date
- Jul 15, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.