FDA recall record

Kenai Red Fish Company Frozen Wild Alaska Smoked Salmon Spread packaged in 6 oz recall — FDA F-1290-2023

The ingredients Statement declares Salmon, Marscapone, Cream Cheese, and Worchester Sauce. The Contains statement declares Fish and Milk but it does not…

Class IIIclassification
F-1290-2023official record ID
Jul 26, 2023report date

Recall record at a glance

Official recordF-1290-2023
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmKenai Red Fish Company LLC
Report dateJul 26, 2023
Recall initiation dateJun 14, 2023
Quantity310 units
LocationPortland, OR, United States

Official product description

Frozen Wild Alaska Smoked Salmon Spread packaged in 6 oz. (net weight) rigid plastic tubs. Product packed in 10 units per case. Product is labeled in part, "***KENAI*RED FISH COMPANY***WILD ALASKA SMOKED SALMON SPREAD KEEP FROZEN - STIR & REFRIGERATE AFTER OPENING Ingredients: Wild Alaska Smoked Salmon (Salmon, Brown Sugar, Salt, Natural Smoke) Marscapone, Cream Cheese, Chives, Salt, Pepper, Lemon, Garlic, Worchester Sauce. CONTAINS: FISH, MILK NET WT. 6 oz (170g)***" The retail store furthers add a white adhesive label that is labeled in part, "***0234476 010991***WILD ALASKAN HOT SMOKED SALMON SPREAD***MARKETOFCHOICE.COM***"

Why the product was recalled

The ingredients Statement declares Salmon, Marscapone, Cream Cheese, and Worchester Sauce. The Contains statement declares Fish and Milk but it does not declare Anchovies and Salmon.

Distribution information

Product distributed in OR.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.