Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish Protein (Pollock Whiting and or Thread... — FDA record F-0991-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 19, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
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)
Reason
Product found to contain undeclared wheat and eggs
Classification
Class I
Recalling firm
Aquamar Inc
Quantity
31,079 cases
Agency-reported status
Terminated
Source record identifier
F-0991-2023

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What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityItem 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

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

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)

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jun 28, 2023
Recall initiation date
May 19, 2023
Center classification date
Jun 20, 2023
Termination date
Jan 7, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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