Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 12, 2015 (11 years ago)

Kirkland Signature Salmon Milano with Basil Pesto Butter approx recall

Recalled by Marine Harvest · Los Angeles, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

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

Quantity: 15,629 units

Food: Seafood & fish

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Arizona California Nevada

FDA's distribution note: U.S. distribution to the following; CA, AZ, and NV. No foreign distribution.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Marine Harvest
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 12, 2015
In FDA report of
Jul 29, 2015
Terminated
Aug 26, 2015
FDA recall number
F-2858-2015 · event 71500
Official record
FDA enforcement report search

Also recalled with it (2 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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