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Food FDA Class I Terminated Pathogen contamination

Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193, net wt. 1lb. Product is packaged in clear plastic clamshell container and sold to consumers.

Western United Fish Company Inc Published Oct 15, 2025

Risk level

Class I

Dangerous or defective — could cause serious health problems or death.

Severity score 95/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Western United Fish Company Inc or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the green onions which were used only in Ahi Tuna Wasabi Poke.

Hazards

Listeria monocytogenes · primary

Affected products (1)

Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193, net wt. 1lb. Product is packaged in clear plastic clamshell container and sold to consumers.

3,314.7 lbs.

Code info: Pack Date of 9/18/2025 Sell By Date of 9/22/2025

Affected areas

AlabamaAlaskaArkansasColoradoConnecticutDelawareFloridaGeorgiaIdahoIllinoisIndianaIowaKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMissouriMontanaNebraskaNew HampshireNew JerseyNew MexicoNew YorkNorth CarolinaOhioOregonPennsylvaniaSouth CarolinaTennesseeTexasUtahVirginiaWashingtonWisconsin

Timeline

  1. Initiated
    Sep 18, 2025
  2. Published
    Oct 15, 2025
  3. Terminated
    Nov 25, 2025
Recall number
H-0023-2026
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.