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Mutual Trading Company Inc. Recall: Imported Monkfish Liver undeclared allergen (Milk)

United States

TerminatedClass I

Company
Mutual Trading Company Inc.
Product
Product is individually packaged in opaque airtight plastic…
Recall date
January 15, 2025
Terminated
July 15, 2025
Source
FDA

Reason for recall

Imported Monkfish Liver undeclared allergen (Milk)

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
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

Distribution

  • Firm distributed product in CT
  • FL
  • GA
  • MA
  • MD
  • NJ
  • NY

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0534-2025
Event ID
96148
Status
Terminated
Classification
Class I
Company
Mutual Trading Company Inc.
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
Quantity
70 cases
Reason
Imported Monkfish Liver undeclared allergen (Milk)
Recall initiation date
January 15, 2025
Report date
February 12, 2025
Classification date
Not published in this source record
Termination date
July 15, 2025
Distribution pattern
Firm distributed product in CT, FL, GA, MA, MD, NJ, NY
UPC, lot, and code information
Two lots: Best By 11/15/2024 Best BY 06/30/2025
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Mutual Trading Company Inc.

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Distribution map

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.

Distribution map
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.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

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.

Is this recall still active?

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.

What should I do if I have this product?

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.

Where can I find more official information?

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