North Coast Traditional Nova Lox, cold smoked salmon, various net wt. 2-3lb average per side. UPC 008603005200. The Ing
Summary
The FDA issued a Class I for North Coast Traditional Nova Lox, cold smoked salmon, various net wt. 2-3lb aver by Oregon Lox Company. Reason: Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0244-2022
Action Date
2021-12-15
Status
Terminated
Category
food
Product Description
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 ***".
Lot/Code Info: 22821
Quantity Affected: 262 lbs.
Reason for Recall
Listeria monocytogenes.
Distribution
distributed in AK, CA, OR, and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-11-11
Company
Eugene, OR
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 60 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Oregon Lox Company has 3 FDA actions in our database, including 3 recalls.
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 (Oregon Lox Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Oregon Lox Company have FDA actions?
Oregon Lox Company has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0244-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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