Marine Harvest Kirkland Signature Salmon Milano with Basil Recall

Why it was recalled

Marine Harvest is recalling raw, fresh, farmed Chilean Atlantic salmon refrigerated salmon fillets due to potential Listeria monocytogenes contamination.

Product description

Kirkland Signature Salmon Milano with Basil Pesto Butter approx 1.5 lbs. Packaged in a metal tray with plastic cover.

Lot numbers, UPCs & expiration codes

Purchase dates of: 05/02-09/15 Item #: 40254

Where it was sold

U.S. distribution to the following; CA, AZ, and NV. No foreign distribution.

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-2858-2015
Classification: Class II
Status: Terminated
Recall initiated: Jun 12, 2015
FDA report date: Jul 29, 2015
Quantity: 15,629 units
Recall type: Voluntary: Firm initiated
Recalling firm: Marine Harvest

Original FDA data

Every field from FDA enforcement report F-2858-2015, exactly as published.

Show all FDA fields

City: Los Angeles
State: CA
Status: Terminated
Country: United States
Event ID: 71500
Address: 3060 E Washington Blvd
Code information: Purchase dates of: 05/02-09/15 Item #: 40254
Postal code: 90023-4220
Report date: Jul 29, 2015
Product type: Food
Recall number: F-2858-2015
Classification: Class II
Recalling firm: Marine Harvest
Product quantity: 15,629 units
Termination date: Aug 26, 2015
Reason for recall: Marine Harvest is recalling raw, fresh, farmed Chilean Atlantic salmon refrigerated salmon fillets due to potential Listeria monocytogenes contamination.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Kirkland Signature Salmon Milano with Basil Pesto Butter approx 1.5 lbs. Packaged in a metal tray with plastic cover.
Distribution pattern: U.S. distribution to the following; CA, AZ, and NV. No foreign distribution.
Recall initiation date: Jun 12, 2015
Initial firm notification: Telephone
Center classification date: Jul 20, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2858-2015, published Jul 29, 2015. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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