Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 6, 2012 (14 years ago)

Pasta Roni Parmesan Cheese Flavor angel hair pasta in a Parmesan… recall

Recalled by Quaker Foods and Snacks North America · Chicago, IL, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Two ingredients used in production of certain Pasta Roni products, were recalled by the supplier due to potential metal fragment contamination associated with the lactic acid used in production of the ingredient.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Pasta Roni Parmesan Cheese Flavor angel hair pasta in a Parmesan sauce with other natural flavors; Net Wt. 5.1 oz. box/12 boxes/case; Distributed by Golden Grain Co., P.O. Box 049003, Chicago, IL 60604-9903; UPC 0 15300 44049

Quantity: 4,331 cases

Food: Cheese Pasta, rice & grains Sauces, dips & dressings

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

UPC 0 15300 44049, Best Before May 11 13, May 12 13, May 16 13 and May 18 13

Where it was sold

Alabama California Connecticut Florida Georgia Illinois Indiana Kentucky Louisiana Ohio Pennsylvania South Carolina Virginia

FDA's distribution note: Alabama, California, Connecticut, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Ohio, Pennsylvania, South Carolina and Virginia.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Quaker Foods and Snacks North America
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 6, 2012
In FDA report of
Jul 4, 2012
Terminated
Dec 14, 2012
FDA recall number
F-1641-2012 · event 62119
Official record
FDA enforcement report search

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