NONNA FOODS Recall: The product may contain undeclared milk due potential product mix-up.

🇺🇸 United States

1. March 9, 2017 - Recall initiated
2. April 19, 2017 - Reported by source
3. August 31, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1860-2017

Event ID

76689

Status

Terminated

Classification

Class I

Company

NONNA FOODS

Product description

LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797

Quantity

750 jars of Lidia's Vodka Sauce were mislabeled as Lidia's Marinara Sauce

Reason

The product may contain undeclared milk due potential product mix-up.

Recall initiation date

March 9, 2017

Report date

April 19, 2017

Classification date

Not published in this source record

Termination date

August 31, 2017

Distribution pattern

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, Indiana, Wisconsin, Illinois, Tennessee, Alabama, Mississippi, Louisiana, Arkansas, Iowa, Minnesota, North Dakota, South Dakota, Nebraska, Texas, Missouri, Kansas, Oklahoma, Colorado, New Mexico, Wyoming, and Montana.

UPC, lot, and code information

UPC 897712001018; Best By Date 06/13/2019 (found on the neck of the jar)

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: NONNA FOODS

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
District of Columbia	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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