RecallHawk
Class I Recall

Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193, net wt. 1lb. Product is packaged in clear plastic clamshel

Western United Fish Company Inc

Summary

The FDA issued a Class I for Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco #17193, net wt. 1lb. Produ by Western United Fish Company Inc. Reason: Listeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the gre.

Details

Source

Food Recall

External ID

H-0023-2026

Action Date

2025-10-15

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 3,314.7 lbs.

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.

Distribution

Product was sold in the following states: AK, AL, AR, CO, CT, DE, FL, GA, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, and WI.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-09-18

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 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Western United Fish Company Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Western United Fish Company Inc have FDA actions?

This is the only FDA action we have on record for Western United Fish Company Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0023-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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