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RECALL RECORD — CLASS IRecall closedF-0990-2023/FDA enforcement
Aquamar INC·Food·May 19, 2023

Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ingredients: Fish Protein (Pollock, …

What you need to know

Class I

  • What happened

    Product found to contain undeclared wheat and eggs

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. Fish-derived ingredients were omitted from the label, creating a risk for fish-allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAAZ, CA, NV, TX +8 moreMore food

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Product identification

Source: FDA FOOD

Brand nameAquamar INC
Recalling firmAquamar INCRancho Cucamonga, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Item 1485 - Surimi Seafood Shred Miyako: Lot numbers (expiration dates): 02/13/23, 03/07/23, 03/14/23, 04/17/23, 05/08/23, 05/23/23, 06/06/23, 06/20/23, 07/10/23, 07/26/23 Item 91403 AS10C ICM Shred 4/2.5Lb KS10-0440-C: Lot numbers (expiration dates) 02/08/23, 11/01/22, 11/29/22, 12/12/22, 12/22/22. Item 91408 KSA ICM Shred 12/2.5Lb KS22-1240-C: Lot numbers (expirations dates) 12/13/23, 02/21/23, 03/28/23, 04/19/23, 05/24/23, 06/26/23, 08/08/23 Item 92407 KS21 ICM Shred 12/2.5Lb KS23-1240-Z, Frozen Lot numbers (production dates julian code) 10223, 03923, 25723, 30522, 23022
Distribution area
AZCANVTXWAGAILMNNCCONJFL

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)

United States

Quantity affected31, 079 cases
Recall initiationFDA report date: June 28, 2023
FDA recall numberF-0990-2023

Beyond the headline

The recall, in context

Aquamar INC initiated this food recall on May 19, 2023. The FDA enforcement report states: Product found to contain undeclared wheat and eggs. The FDA report lists distribution as: 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).

The FDA enforcement report describes the reason as: Product found to contain undeclared wheat and eggs

Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ingredients: Fish Protein (Pollock, … was made or distributed by Aquamar INC in Rancho Cucamonga, CA, United States. This page reflects FDA report F-0990-2023, dated June 28, 2023.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared fish

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a fish allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ingredients: Fish Protein (Pollock, … recall?

Aquamar INC recalled Miyako Select Shredded Crab Meat Keep Refrigerated #1485 Ingredients: Fish Protein (Pollock, … in an FDA Class I enforcement action reported as F-0990-2023. Product found to contain undeclared wheat and eggs

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a fish allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Aquamar INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0990-2023. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Aquamar INC

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Class I·

Aquamar INC

Kanimi Crab Flavored Seafood Fancy Shred Style 92410 Ingredients: Fish Protein (Pollock, …

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Class I·

Aquamar INC

Kanimi Easy Roll Crab Flavored Seafood Shred Style 91406 Vcm Ingredients: Fish Protein (Pollock…

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.