FDA recall record

New Seasons Market Grab and Go Pre-Packaged Macaroni and recall — FDA F-0559-2018

New Seasons Market Grab and Go Pre-Packaged Macaroni and Cheese is recalled due to undeclared egg.

Class Iclassification
F-0559-2018official record ID
Jan 17, 2018report date

Recall record at a glance

Official recordF-0559-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmNEW SEASONS MARKET
Report dateJan 17, 2018
Recall initiation dateDec 28, 2017
Quantity924 small packages and 911 Large packages
LocationPortland, OR, United States

Official product description

New Seasons Market Grab and Go Pre-Packaged Macaroni and Cheese - refrigerated. Product is packaged in aluminum shallow containers with a clear plastic dome lid and sold in two sizes: Small package UPC 252089 203999. Large package UPC 252090 706991. The label is read in parts: "***NEW SEASONS MARKET MACARONI & CHEESE***Pasta [water, enriched durum semolina durum semolina wheat flour, niacin, ferrous sulfate, thiamine mononitrate, riboflavin, folic acid)], Mac and Cheese sauce [milk (grade A pasteurized milk, vitamin A palmitate, vitamin D3), medium cheddar cheese [cultured milk, salt, enzymes, annatto (color), potato starch and cellulose powder (added to prevent caking), natamycin (natural mold inhibitor)], wheat flour (unbleached wheat flour, niacin, iron, thiamin mononitrate, riboflavin, folic acid), unsalted butter***Contains: Wheat, Milk***".

Why the product was recalled

New Seasons Market Grab and Go Pre-Packaged Macaroni and Cheese is recalled due to undeclared egg.

Distribution information

distributed in CA, OR, and WA

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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