La Terra Fina Dip Recall: Undeclared Egg Allergen
La Terra Fina recalls Spinach Artichoke & Parmesan Dip due to undeclared egg. Check your UPC and lot number for details on this Class I food recall.
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Undeclared allergen; egg.
Contact the company
What happened, in plain English
La Terra Fina, Inc. is recalling its Spinach Artichoke & Parmesan Dip & Spread because it contains undeclared egg. This is a Class I recall, indicating the highest risk of adverse health consequences. The product was distributed in multiple U.S. states including California, New Jersey, and Texas. Read more at govinfonow.com/recall/20375-la-terra-fina-dip-recall-undeclared-egg-allergen.
Source Summary by GovInfoNow · govinfonow.com/recall/20375-la-terra-fina-dip-recall-undeclared-egg-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-0024-2018
Cite this page
“La Terra Fina Dip Recall: Undeclared Egg Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/20375-la-terra-fina-dip-recall-undeclared-egg-allergen. Based on FDA recall #F-0024-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0024-2018%22&limit=1).
Why it’s dangerous
The product contains undeclared egg, which is a major food allergen. For people with egg allergies, consuming this dip can trigger a serious allergic reaction or other acute health issues.
Who’s affected
Consumers who purchased the recalled dip at retailers in CA, NJ, CO, GA, FL, MD, PA, MA, IN, WI, TX, and NY. Individuals with egg allergies are at the highest risk of an allergic reaction.
How to tell if you have this one
Look for La Terra Fina Spinach Artichoke & Parmesan Dip & Spread in 10 oz (284g) containers. Check the UPC code 6-40410-51327-3 and the lot number 20170912 with a Use By Date of NOV-01-2017.
- Brand
La Terra Fina- Product
La Terra Fina Spinach Artichoke & Parmesan Dip & Spread NET WT. 10 oz. (.625 lb.) 284g UPC 6-40410-51327-3- Category
Food
What to do — step by step
Check Your Product
Verify if your dip matches the UPC 6-40410-51327-3 and lot number 20170912.
Stop Consumption
Do not eat the product if it matches the recalled details due to the undeclared egg allergen.
Where it went and when
Where it was distributed
Distributed in 12 states.
FDA distribution: “U.S. distribution to the following: CA, NJ, CO, GA, FL, MD, PA, MA, IN, WI, TX, and NY. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Florida, Georgia, Indiana, Maryland, Massachusetts, New Jersey, New York, Pennsylvania, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 56 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-0024-2018 (October 10, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0024-2018 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.