High Liner Foods Breaded Shrimp Recall: Undeclared Milk and Eggs
High Liner Foods recalls breaded shrimp products containing undeclared milk and eggs. Consumers should check lot numbers 0046351131 and 0046351230 for affected items.
Lower-risk recall
Product contains undeclared milk and eggs
Contact the company
What happened, in plain English
High Liner Foods is recalling breaded shrimp products that contain undeclared milk and eggs. This poses a risk for people with allergies to milk or eggs, as the product was not labeled to indicate these ingredients. Read more at govinfonow.com/recall/22469-high-liner-foods-breaded-shrimp-recall-undeclared-milk-and-eggs.
Source Summary by GovInfoNow · govinfonow.com/recall/22469-high-liner-foods-breaded-shrimp-recall-undeclared-milk-and-eggs · Updated October 8, 2026 · FDA enforcement record: FDA #F-1295-2017
Cite this page
“High Liner Foods Breaded Shrimp Recall: Undeclared Milk and Eggs.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22469-high-liner-foods-breaded-shrimp-recall-undeclared-milk-and-eggs. Based on FDA recall #F-1295-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1295-2017%22&limit=1).
Why it’s dangerous
The shrimp products contain milk and eggs without being declared on the label. This can cause allergic reactions in individuals sensitive to these ingredients, which may include hives, swelling, or more severe reactions.
Who’s affected
People with milk or egg allergies are most at risk from this recall. Anyone who purchased the recalled shrimp products should check their lot numbers.
How to tell if you have this one
Check for lot numbers 0046351131 or 0046351230 on the packaging. The product is a 12-8 oz. carton per master case, with the master case weighing 6 lbs.
- Brand
High Liner Foods- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot numbers 0046351131 or 0046351230 on the packaging.
Where it went and when
Where it was distributed
Distributed in 7 states.
FDA distribution: “The distribution is specifically in the United States (VA, IL, MD, IN, WI, MI, NJ)” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Indiana, Maryland, Michigan, New Jersey, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 36 days 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-1295-2017 (January 3, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1295-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.