Nonna Foods LIDIA'S MARINARA Recall: Undeclared Milk Risk
Nonna Foods recalls LIDIA'S MARINARA sauce due to potential undeclared milk in some batches. Consumers should check UPC 897712001018 and contact for details.
Lower-risk recall
The product may contain undeclared milk due potential product mix-up.
Contact the company
What happened, in plain English
Nonna Foods is recalling LIDIA'S MARINARA sauce (25 oz) because it may contain undeclared milk from a product mix-up. This could affect people with milk allergies or sensitivities. Read more at govinfonow.com/recall/22020-nonna-foods-lidia-s-marinara-recall-undeclared-milk-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/22020-nonna-foods-lidia-s-marinara-recall-undeclared-milk-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-1860-2017
Cite this page
“Nonna Foods LIDIA'S MARINARA Recall: Undeclared Milk Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22020-nonna-foods-lidia-s-marinara-recall-undeclared-milk-risk. Based on FDA recall #F-1860-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1860-2017%22&limit=1).
Why it’s dangerous
The sauce may contain undeclared milk due to a product mix-up during manufacturing. This poses a risk for individuals with milk allergies or sensitivities, as they could experience adverse reactions.
Who’s affected
People who own or use this sauce are most at risk if they have milk allergies or sensitivities. The recall applies to consumers who purchased the product with the specific UPC code.
How to tell if you have this one
Check for the UPC 897712001018 on the jar. The product was manufactured for Nonna Foods LLC in Woodbury, NY and has a best by date of 06/13/2019.
- Brand
Nonna Foods- Product
LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797- Category
Food
What to do — step by step
Check Product Details
Look for the UPC 897712001018 on the jar to confirm if it's the recalled product.
Where it went and when
Where it was distributed
Distributed in 40 states and D.C..
FDA distribution: “New York, New Jersey, Connecticut, Rhode Island, New Hampshire, Massachusetts, Maine, Vermont, Pennsylvania, Delaware, Maryland, West Virginia, Virginia, Washington DC, North Carolina, South Carolina, Kentucky, Florida, Ohio, Michigan,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arkansas, Colorado, Connecticut, Delaware, District of Columbia, Florida, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Vermont, Virginia, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA terminated this recall 6 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-1860-2017 (March 9, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1860-2017 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.