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Lower risk Food recall · FDA · Published October 30, 2019

Tony's Columbia Gorge Salmon Recall: Under-processed Canned Salmon Risk

Tony's Smoke House recalls Columbia Gorge Salmon due to possible under-processing. Canned salmon may have firm cans with missing lot codes. Consumers should check labels for lot 4 05019.

🇺🇸 FDA recall #F-0154-2020FoodTony's Smoke House ›
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Contact the company

Recalling firmTonys Smoke House and Cannery Inc1316 Washington St · Oregon City, OR 97045-1649
✎ GovInfoNow plain-language explainer

Tony's Smoke House recalled skinless and boneless salmon in metal cans (6.5 oz) because it may have been under-processed. This could lead to unsafe food if the can is firm and the lot code isn't found in their records. Read more at govinfonow.com/recall/16450-tony-s-columbia-gorge-salmon-recall-under-processed-canned-salmon.

Source Summary by GovInfoNow · govinfonow.com/recall/16450-tony-s-columbia-gorge-salmon-recall-under-processed-canned-salmon · Updated October 5, 2026 · FDA enforcement record: FDA #F-0154-2020

Cite this page

“Tony's Columbia Gorge Salmon Recall: Under-processed Canned Salmon Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16450-tony-s-columbia-gorge-salmon-recall-under-processed-canned-salmon. Based on FDA recall #F-0154-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0154-2020%22&limit=1).

The FDA announced on Oct. 30, 2019, that Tony's Smoke House and Cannery Inc voluntarily recalled canned salmon products due to potential under-processing. The recall affects 6 cans distributed in Oregon.

How to tell if you have it

  • Brand: Tony's Smoke House
  • Product: Tony's Columbia Gorge Salmon, Skinless and boneless salmon
  • Packaging: Metal can, Net Wt. 6.5 oz./184g
  • Lot code: 4 05019
  • Quantity: 6 cans
  • Distribution: OR only

The hazard

The canned salmon product was recalled because it may have been under-processed. The firm could not find the lot code in their canning records.

Context

GovInfoNow's records show other recent recalls of similar products include Albertsons Salmon Atlantic Portion with Orange Marinade Recall (2026-05-06), Albertsons Burger Wild Salmon Feta Spinach Recall (2026-05-06), and Wellsley Farms Salmon Recall (2026-02-10).

How to tell if you have this one

Check for the label with "Columbia Gorge Salmon" and the lot code 4 05019 on the can. The product is packaged in a metal can with a net weight of 6.5 oz/184g.

  • Brand
    Tony's Smoke House
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label

    Look for the lot code 4 05019 on the can's label to confirm if it's recalled.

Where it went and when

Where it was distributed

Distributed in Oregon.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “distributed in OR only” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon.

Recall timeline

FDA terminated this recall 49 days after the firm started it.

1. Firm started the recall: Oct 30, 201912. FDA classified it Class II: Nov 14, 201923. Published in FDA’s Enforcement Report: Nov 20, 201934. FDA terminated the recall: Dec 18, 201942019
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0154-2020 (October 30, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0154-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA