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High RiskFDAfda-F-0826-2017UNDECLARED ALLERGEN

PREMIUM SMOKED SALMON UPC 7 02772 00564 0 Packaged in a 5 lb case 20/4oz vacuum packaged per case. Cardboard type label is folded ove...

Category
Units Affected
28,487
Recall Date
November 10, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0826-2017.

Northern Fish Products is recalling hot smoked salmon, black cod, steelhead, and trout, with the exception of hot jerky salmon and jerky salmon due to undeclared soy.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0826-2017.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Northern Fish Products, Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-0826-2017.

Northern Fish Products, Inc.

FDA

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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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📣 Report a food, supplement, or cosmetic problem to the FDA

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.

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Northern Fish Products, Inc. Recall FAQ

Northern Fish Products, Inc. is the subject of a seafood safety report: PREMIUM SMOKED SALMON UPC 7 02772 00564 0 Packaged in a 5 lb case 20/4oz vacuum packaged per case. Cardboard type label is folded ove.... The notice was published on November 10, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 28,487 units are potentially affected.