Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite side
Summary
The FDA issued a Class I for Product is individually packaged in opaque airtight plastic packaging with Chine by Mutual Trading Company Inc.. Reason: Imported Monkfish Liver undeclared allergen (Milk).
Details
Source
Food Recall
External ID
F-0534-2025
Action Date
2025-02-12
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Two lots: Best By 11/15/2024 Best BY 06/30/2025
Quantity Affected: 70 cases
Reason for Recall
Imported Monkfish Liver undeclared allergen (Milk)
Distribution
Firm distributed product in CT, FL, GA, MA, MD, NJ, NY
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-15
Company
El Monte, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 106 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mutual Trading Company Inc. has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mutual Trading Company Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mutual Trading Company Inc. have FDA actions?
Mutual Trading Company Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0534-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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