Food recall

B&G Foods North America, Inc recall: Victoria Marinara Sauce

B&G Foods North America, Inc, of Parsippany, NJ, recalled Victoria Marinara Sauce. The FDA's reason: “Product may contain undeclared cashews.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on February 20, 2019, and the FDA first listed it in its Enforcement Report of March 20, 2019. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class I

It could cause serious harm or death

Why

Allergen not on the label

Status

Terminated

Closed September 1, 2021

The recall

Company
B&G Foods North America, Inc (Parsippany, NJ)
Reason, in FDA's words
“Product may contain undeclared cashews.”
Where it was sold
The product was distributed to the following States: CT, NJ, NY, PA
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
82238

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-1184-2019 Class I

    Victoria Marinara Sauce, 40 oz. (2.5 lb) 1133g, 6Jars / Case

    Codes: Best By 03/06/2022

    Quantity: 1,280 Cases

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of March 20, 2019.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.