Food Recall Check
Class I · High risk Terminated Initiated Nov 11, 2021 (5 years ago)

North Coast Traditional Nova Lox recall

Recalled by Oregon Lox Company · Eugene, OR, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Listeria monocytogenes.

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

North Coast Traditional Nova Lox, cold smoked salmon, various net wt. 2-3lb average per side. UPC 008603005200. The Ingredients statement on the label are read in parts: "***INGREDIENTS: Wild Pacific salmon, corn oil, salt, brown sugar, sodium nitrite, FD&C Yellow 6/Red 40, natural hardwood smoke ***CONTAINS: Keta Salmon (Fish) ***KEEP FROZEN OR STORE BELOW 38F ***".

Quantity: 262 lbs.

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.

22821

Where it was sold

Alaska California Oregon Washington

FDA's distribution note: distributed in AK, CA, OR, and WA.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Oregon Lox Company
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 11, 2021
In FDA report of
Dec 15, 2021
Terminated
Dec 16, 2021
FDA recall number
F-0244-2022 · event 89038
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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