FDA recall record

New Seasons Market 9 inch Asparagus and Goat Cheese Quiche, packaged in a recall — FDA F-0916-2018

9 inch Asparagus and Goat Cheese Quiche is recalled because egg is declared in the Ingredients statement but it is not declared in the Contains statement.

Class IIclassification
F-0916-2018official record ID
Mar 21, 2018report date

Recall record at a glance

Official recordF-0916-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNew Seasons Market LLC
Report dateMar 21, 2018
Recall initiation dateMar 5, 2018
Quantity45 units
LocationPortland, OR, United States

Official product description

9 inch Asparagus and Goat Cheese Quiche, packaged in a cardboard box with a clear window. UPC # 2 52209 10599 8. The retail label is read in parts: "***ASPARAGUS GOAT CHEESE QUICHE ***NEW SEASONS MARKET***Egg, whole milk, fresh goat cheese, sour cream (milk, cream, nonfat dry milk, enzyme), asparagus, salt, pie shell (wheat flour, canola oil, modified palm oil shortening, water, cornstarch, corn flour, dextrose, salt, soy lecithin, protease enzyme, sodium propionate)***Contains: WHEAT, SOY, MILK.

Why the product was recalled

9 inch Asparagus and Goat Cheese Quiche is recalled because egg is declared in the Ingredients statement but it is not declared in the Contains statement.

Distribution information

distributed in Oregon and Washington

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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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