COLUMBIA RIVER SOCKEYE (Old label) Canned Sockeye Salmon with paper label reading in part: ***SKIPANON BRAND…
Food recall F-0386-2016. Published in FDA’s Enforcement Report on Dec 16, 2015.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Dec 16, 2015. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 4 states named
- approximately 57,000 cans total how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
All cans and pouches of Skipanon Brand seafood, including salmon products are being recalled due to lack of documentation and possible under-processed product. Under-processed seafood could lead to contamination with Clostridium botulinum.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
COLUMBIA RIVER SOCKEYE (Old label) Canned Sockeye Salmon with paper label reading in part: ***SKIPANON BRAND DELUXE HANDFILLED COLUMBIA RIVER SOCKEYE*** Ingredients: Sockeye Salmon, Salt NET WT. 6 OZ. (170g)*** UPC: 58071 00120 Label has green and yellow background with a red border and multiple colored ink lettering. SOCKEYE SALMON (New label) Canned Sockeye Salmon with paper label reading in part: ***SKIPANON BRAND SEAFOOD SOCKEYE SALMON***Ingredients: Sockeye Salmon, Sea Salt. NET wt. 6 oz. (170g)***” UPC: 58071 00120 Can code beginning with OCBB Label has a yellow background with a blue/gray stripe on the bottom and multiple colored ink lettering.
approximately 57,000 cans total, in FDA’s words.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
All lots
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Barcodes and drug codes
-
UPC
5807100120
As FDA’s description and codes give them; the UPCs written as digits only.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
No Foreign Consignees No VA or DoD Consignees. Distributed to Michigan, Nevada, Oregon, and Washington and sold to internet customers nationwide from the website skipanonbrand.com.
The states and territories these words name
- Michigan
- Nevada
- Oregon
- Washington
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Oct 9, 2015.
- FDA classified it on Dec 10, 2015.
- FDA’s Enforcement Report published it on Dec 16, 2015.
- FDA terminated it on Jun 26, 2017.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Skipanon Brand Seafoods LLC, of Warrenton, OR.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
FDA, Food recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- Meat, poultry and egg products are recalled by USDA’s Food Safety and Inspection Service, not FDA, and its recalls aren’t here yet: see fsis.usda.gov.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Food recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.