Sullivan Harbor Farm Cold Smoked Salmon Recall: Low Water Phase Salt Hazard
Mill Stream Corp. recalls Sullivan Harbor Farm Cold Smoked Salmon due to low water phase salt. Products sold in vacuum packaging (4oz, 8oz, 1lb, 2lb) with specific UPCs. Consumers should check labels for affected items.
Lower-risk recall
Low water phase salt.
Contact the company
What happened, in plain English
Mill Stream Corp. is recalling Sullivan Harbor Farm Cold Smoked Salmon products that may contain low water phase salt. This issue could lead to food safety concerns if the product is consumed without proper salt levels. Read more at govinfonow.com/recall/16325-sullivan-harbor-farm-cold-smoked-salmon-recall-low-water-phase.
Source Summary by GovInfoNow · govinfonow.com/recall/16325-sullivan-harbor-farm-cold-smoked-salmon-recall-low-water-phase · Updated October 5, 2026 · FDA enforcement record: FDA #F-0203-2020
Cite this page
“Sullivan Harbor Farm Cold Smoked Salmon Recall: Low Water Phase Salt Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16325-sullivan-harbor-farm-cold-smoked-salmon-recall-low-water-phase. Based on FDA recall #F-0203-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0203-2020%22&limit=1).
Why it’s dangerous
Low water phase salt in the product could affect the food's safety and quality. This may lead to issues with the product's shelf life or taste if consumed without proper salt levels.
Who’s affected
Consumers who purchased Sullivan Harbor Farm Cold Smoked Salmon in vacuum packaging (4 oz., 8 oz., 1 lb., 2 lb., or whole sides) from stores that sold these products. Those with specific UPC codes listed are most at risk.
How to tell if you have this one
Check for vacuum packaging with 4 oz., 8 oz., 1 lb., 2 lb., or whole sides labels. Look for UPC codes 1218700003 (4 oz) and 1218700001 (8 oz).
- Brand
Sullivan Harbor Farm Smokehouse- Category
Food
What to do — step by step
Check Product Labels
Look for vacuum packaging with 4 oz., 8 oz., 1 lb., 2 lb., or whole sides labels and specific UPC codes.
Where it went and when
Where it was distributed
Distributed in 23 states.
FDA distribution: “CO,TX,CT,OH,FL,ME,NJ,UT,IA,TN,MN,VA,IL,NH,MA,VT,PA,AZ,NY,RI,MI,WI,GA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Colorado, Connecticut, Florida, Georgia, Illinois, Iowa, Maine, Massachusetts, Michigan, Minnesota, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Tennessee, Texas, Utah, Vermont, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 3 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-0203-2020 (November 4, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0203-2020 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.