Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Frozen Wild Alaska Smoked Salmon Spread packaged in recall
Recalled by Kenai Red Fish Company LLC · Portland, OR, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it 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.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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***"
Quantity: 310 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.
The product is not labeled with manufacturing codes.
Where it was sold
Oregon
FDA's distribution note: Product distributed in OR.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
- Kenai Red Fish Company LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 14, 2023
- In FDA report of
- Jul 26, 2023
- Terminated
- Oct 3, 2023
- FDA recall number
- F-1290-2023 · event 92574
- Official record
- FDA enforcement report search
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