Class ITerminatedVoluntary: Firm initiated
Mutual Trading Company Inc.: food recall F-0534-2025
Mutual Trading Company Inc. of El Monte, CA recalled Product is individually packaged in opaque airtight plastic packaging with Chinese lettering on one side. Opposite… Reason: Imported Monkfish Liver undeclared allergen (Milk). The FDA listed it as Class I in its Enforcement Report dated Feb 12, 2025; distribution: Connecticut, Florida, Georgia, Massachusetts, Maryland, New Jersey, New York.
Record status as published: Terminated (terminated Jul 15, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- 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
- Product quantity
- 70 cases
- Reason for recall
- Imported Monkfish Liver undeclared allergen (Milk)
- Codes, lots and dates on the package
- Two lots: Best By 11/15/2024 Best BY 06/30/2025
- Distribution pattern
- Firm distributed product in CT, FL, GA, MA, MD, NJ, NY
- Recalling firm
- Mutual Trading Company Inc., El Monte, CA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jan 15, 2025 |
| Classified by the FDA | Feb 6, 2025 |
| Published in the Enforcement Report | Feb 12, 2025 |
| Terminated | Jul 15, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0534-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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