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Class ITerminated in FDA datasetRecall initiated May 19, 2023

Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM

Recalling firm: Aquamar Inc

Why it was recalled

Product found to contain undeclared wheat and eggs

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 7, 2025.

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ProductKanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish Protein (Pollock Whiting and or Threadfin Bream), Water, Potato Starch, Contains less than 2% of the following: Sugar, Modified Food Starch, Liquid Egg White, Salt, Sorbitol, Natural and Artificial Flavors (Hydrolyzed Soy Protein, Crab Extract), Carrageenan, Sodium Tripolyphosphate, Tetrasodium Pyrophosphate, Carmine, Natural and Artificial Color. Contains: Fish (Pollock, Whiting and Threadfin Bream) Soy, Crustacean Shellfish (Swimming Crab), Eggs 30 lbs. (12 packages/2.5 lb vacuum sealed in clear film, pasteurized)
Package size30 lbs

FDA code information

Item 91406 VCM Kanimi Easy Roll Mix 12/2.5 lb. Refrigerated. Lot numbers (Expiration dates) 12/18/22, 01/12/23, 01/25/23, 02/21/23, 05/15/23, 05/29/23, 06/06/23, 07/18/23

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Full FDA record and distribution details

Original product description

Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish Protein (Pollock Whiting and or Threadfin Bream), Water, Potato Starch, Contains less than 2% of the following: Sugar, Modified Food Starch, Liquid Egg White, Salt, Sorbitol, Natural and Artificial Flavors (Hydrolyzed Soy Protein, Crab Extract), Carrageenan, Sodium Tripolyphosphate, Tetrasodium Pyrophosphate, Carmine, Natural and Artificial Color. Contains: Fish (Pollock, Whiting and Threadfin Bream) Soy, Crustacean Shellfish (Swimming Crab), Eggs 30 lbs. (12 packages/2.5 lb vacuum sealed in clear film, pasteurized)

Original FDA recall reason

Product found to contain undeclared wheat and eggs

Recall details

Recall number
F-0991-2023
Event ID
92381
FDA status
Terminated
Initiated
May 19, 2023
Reported
Jun 28, 2023
Classified
Jun 20, 2023
Terminated
Jan 7, 2025
Quantity
31,079 cases
Location
Rancho Cucamonga, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

U.S. distribution to the following: AZ, CA, NV, TX, WA, GA, IL, MN, NC, CO, NJ, FL Foreign distribution to the following: CA (British Columbia, Alberta)

FDA source record · F-0991-2023

Data updated September 16, 2026. View official FDA data ↗

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