Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish Protein (Pollock Whiting and or Threadfin
Summary
The FDA issued a Class I for Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 VCM Ingredients: Fish P by Aquamar Inc. Reason: Product found to contain undeclared wheat and eggs.
Details
Source
Food Recall
External ID
F-0991-2023
Action Date
2023-06-28
Status
Terminated
Category
food
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)
Lot/Code Info: 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
Quantity Affected: 31,079 cases
Reason for Recall
Product found to contain undeclared wheat and eggs
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)
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-19
Company
Rancho Cucamonga, 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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Aquamar Inc has 3 FDA actions in our database, including 3 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 (Aquamar Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Aquamar Inc have FDA actions?
Aquamar Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0991-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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