RecallHawk
Class III Recall

Frozen Wild Alaska Smoked Salmon Spread packaged in 6 oz. (net weight) rigid plastic tubs. Product packed in 10 units pe

Kenai Red Fish Company LLC

Summary

The FDA issued a Class III for Frozen Wild Alaska Smoked Salmon Spread packaged in 6 oz. (net weight) rigid pla by Kenai Red Fish Company LLC. Reason: The ingredients Statement declares Salmon, Marscapone, Cream Cheese, and Worchester Sauce. The Contains statement declares Fish and Milk but it does n.

Details

Source

Food Recall

External ID

F-1290-2023

Action Date

2023-07-26

Status

Terminated

Category

food

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***"

Lot/Code Info: The product is not labeled with manufacturing codes.

Quantity Affected: 310 units

Reason for Recall

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

Product distributed in OR.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-14

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 61 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Kenai Red Fish Company LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Kenai Red Fish Company LLC have FDA actions?

This is the only FDA action we have on record for Kenai Red Fish Company LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1290-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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