Seabear Cold Smoked Salmon Recall: Water Phase Salt Deviations and Mislabeling
Seabear Company recalls Cold Smoked Wild Coho Salmon Lox due to water phase salt deviations and mislabeling of storage instructions. Products may not be safe if stored incorrectly.
Lower-risk recall
Products recalled due to water phase salt deviations and mislabeling of storage instructions on finished products labels
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What happened, in plain English
Seabear Company is recalling Cold Smoked Wild Coho Salmon Lox because of water phase salt deviations and mislabeling of storage instructions. This could lead to unsafe conditions if the product is not stored properly. Read more at govinfonow.com/recall/19224-seabear-cold-smoked-salmon-recall-water-phase-salt-deviations-and.
Source Summary by GovInfoNow · govinfonow.com/recall/19224-seabear-cold-smoked-salmon-recall-water-phase-salt-deviations-and · Updated October 7, 2026 · FDA enforcement record: FDA #F-1127-2018
Cite this page
“Seabear Cold Smoked Salmon Recall: Water Phase Salt Deviations and Mislabeling.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19224-seabear-cold-smoked-salmon-recall-water-phase-salt-deviations-and. Based on FDA recall #F-1127-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1127-2018%22&limit=1).
Why it’s dangerous
The product has water phase salt deviations and mislabeled storage instructions. If stored above 38°F, the product may become unsafe due to improper temperature conditions.
Who’s affected
Owners of the recalled Cold Smoked Wild Coho Salmon Lox from Seabear Company, particularly those who store it at temperatures above 38°F. Those who have already thawed the product are at higher risk.
How to tell if you have this one
Look for the product labeled 'Cold Smoked Wild Coho Salmon Lox' by Gerard & Dominique Seafoods with Reduced Oxygen Packaging, 3 oz (85g) net weight. The UPC is 7 52047 92635 4. The package label states 'KEEP REFRIGERATED AT OR BELOW 38 F' and the master case label says 'Important, keep frozen until used, thaw under refrigeration at 38 F or below. Use By 30 days After Thaw'.
- Brand
Seabear Company- Product
Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoods brand, Reduced Oxygen Packaging, Net Wt. 3 oz (85g). UPC- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
nationwide
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1126-2018 | Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Oxygen Packaging, Net Wt. 4oz (113g). No UPC.; Lot #17338/17340. Code is interepreted as follows: Julian Date Code. Lot: 17 =Year 2017 338 = Day (December 4th) Pack Date is 17340, which is also in Julian Date coding. | 381/4 oz. units |
| F-1127-2018 | Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoods brand, Reduced Oxygen Packaging, Net Wt. 3 oz (85g). UPC 7 52047 92635 4. The package label of the Cold Smoked Coho Salmon bears this instructions "***KEEP REFRIGERATED AT OR BELOW 38 F***". The master case label of the Cold Smoked Coho Salmon bears this instructions: "***Important, keep frozen until used, thaw under refrigeration at 38 F or below. Use By 30 days After Thaw***".; Lot # CSCO-17339/Pack Date 17340. Code is interpreted as follows: CS=Cold Smoked CO=Coho. Julian Date Code-Lot: 17=Year 2017, 339=Day (December 5th) Pack Date is 17340, which is also in Julian Date coding | 2080/3 oz. units total |
What to do — step by step
Check Storage Conditions
Ensure the product is stored at or below 38°F if refrigerated or frozen as per the label instructions.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- 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-1127-2018 (April 11, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1127-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.