Food Recall Check
Class I · High risk Terminated Initiated Apr 7, 2015 (12 years ago)

Central Market Teriyaki Salmon Jerky recall

Recalled by World Wide Gourmet Foods, Inc. dba Alaska Smokehouse · Woodinville, WA, United States

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

Why it was recalled

Central Market Teriyaki Salmon Jerkey is recalled due to undeclared soy and wheat.

Undeclared allergens: Soy Wheat Fish

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Central Market Teriyaki Salmon Jerky, 3 oz. per plastic retail pouch. The front label is correctly identified as Teriyaki Salmon Jerky, but the back side was mis-labeled as Smoked Salmon Jerky with the UPC 0 41220 34270 9.

Quantity: 2916 packages (3 oz. per package)

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.

Best by Date: 08/25/2015

Where it was sold

Texas

FDA's distribution note: Distributed in Texas only

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. The risk from an undeclared allergen is to people allergic to soy, wheat, fish; for anyone else the product is generally not a safety concern. 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
World Wide Gourmet Foods, Inc. dba Alaska Smokehouse
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 7, 2015
In FDA report of
May 20, 2015
Terminated
Jul 13, 2015
FDA recall number
F-2256-2015 · event 70935
Official record
FDA enforcement report search

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