FDA recall record

Tonys Smoke House and Cannery Tony's Columbia Gorge Salmon, Skinless and boneless salmon recall — FDA F-0154-2020

Canned salmon product was recalled because it may have been under-processed and firm can't find the lot code in their canning records.

Class IIclassification
F-0154-2020official record ID
Nov 20, 2019report date

Recall record at a glance

Official recordF-0154-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTonys Smoke House and Cannery Inc.
Report dateNov 20, 2019
Recall initiation dateOct 30, 2019
Quantity6 cans
LocationOregon City, OR, United States

Official product description

Tony's Columbia Gorge Salmon, Skinless and boneless salmon, packaged in a metal can, Net Wt. 6.5 oz./184g. The label reads in parts: "*** Columbia Gorge Salmon *** Ingredients: Salmon and Salt ***TONY'S SMOKEHOUSE AND CANNERY 1316 Washington Street Oregon City, OR 97045 United States of America***".

Why the product was recalled

Canned salmon product was recalled because it may have been under-processed and firm can't find the lot code in their canning records.

Distribution information

distributed in OR only

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Other.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.