CLASS I Food recall · Reported 20 May 2015 · FDA Enforcement Report

Central Market Teriyaki Salmon Jerky recalled

World Wide Gourmet Foods is recalling Central Market Teriyaki Salmon Jerky per, distributed in Texas. The recall was initiated on 7 Apr 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest by Date: 08/25/2015
Quantity recalled2916 packages (3 oz. per package)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2256-2015
FDA event ID
70935
Recalling firm
World Wide Gourmet Foods, Woodinville, WA
Brand
Central
Classification
Class I
Status
Terminated
Recall initiated
7 Apr 2015
FDA classified
12 May 2015
Reported
20 May 2015
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Product category
Jerky

Timeline

7 Apr 2015Recall initiated by company
12 May 2015Classified by FDA+35 days
20 May 2015Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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.

Where it was distributed

Distributed in Texas only

Texas

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Best by Date: 08/25/2015

Where was it sold?

Distributed in Texas only

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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