Food FDA Class I Terminated Undeclared allergen
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), UP
Mutual Trading Company Inc. Published Feb 12, 2025
Risk level
Class IDangerous or defective — could cause serious health problems or death.
Severity score 87/100
What should you do?
- Check whether you have this product, using the lot codes, UPCs, and dates listed below.
- If you are allergic or sensitive to the ingredient noted, do not eat it — it could cause a serious reaction.
- Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
- Contact Mutual Trading Company Inc. or your place of purchase with questions, and see the source record below for full details.
Reason for recall
Imported Monkfish Liver undeclared allergen (Milk)
Hazards
Milk · primary
Affected products (1)
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
70 cases
Code info: Two lots: Best By 11/15/2024 Best BY 06/30/2025
Affected areas
ConnecticutFloridaGeorgiaMarylandMassachusettsNew JerseyNew York
Timeline
- InitiatedJan 15, 2025
- PublishedFeb 12, 2025
- TerminatedJul 15, 2025
- Recall number
- F-0534-2025
- Agency
- U.S. Food and Drug Administration
- Country
- US
FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.