Food recall

Veggie Noodle Co recall: Veggie Noodle Co

Veggie Noodle Co, of Austin, TX, recalled Veggie Noodle Co. The FDA's reason: “Possible Listeria monocytogenes contamination.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on February 14, 2017, and the FDA first listed it in its Enforcement Report of March 29, 2017. 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

Listeria

Status

Terminated

Closed March 30, 2017

The recall

Company
Veggie Noodle Co (Austin, TX)
Reason, in FDA's words
“Possible Listeria monocytogenes contamination”
Where it was sold
IL, IN, IA, MI, MN, MO, NE, OH, WI
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
76496

The product recalled

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

  • F-1630-2017 Class I

    Veggie Noodle Co. Butternut Spirals in 10.7 ounce clear plastic containers, UPC: 852287006059 Manufactured By Veggie Noodle Co., LLC. Austin TX 78744

    Codes: Enjoy by: February 23, 2017

    Quantity: 62 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 29, 2017.

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.