Central Market Teriyaki Salmon Jerky, 3 oz. per plastic retail pouch. The front label is correctly identified as Teriyaki Salmon Jer...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2256-2015.
Central Market Teriyaki Salmon Jerkey is recalled due to undeclared soy and wheat.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2256-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact World Wide Gourmet Foods, Inc. Dba Alaska Smokehouse or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2256-2015.
World Wide Gourmet Foods, Inc. dba Alaska Smokehouse
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
World Wide Gourmet Foods, Inc. Dba Alaska Smokehouse Recall FAQ
World Wide Gourmet Foods, Inc. Dba Alaska Smokehouse is the subject of a seafood safety report: Central Market Teriyaki Salmon Jerky, 3 oz. per plastic retail pouch. The front label is correctly identified as Teriyaki Salmon Jer.... The notice was published on April 7, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 2,916 units are potentially affected.