Class ITerminated in FDA datasetRecall initiated Dec 4, 2020

Market of Choice brand Sour Cherry Baked Brie is wrapped in a plastic shrink wrap and has a…

Recalling firm: Market of Choice Inc

Why it was recalled

Sour Cherry Baked Brie was recalled because the scale label, which was printed at retail stores, do not list almond.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 6, 2021.

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ProductMarket of Choice brand Sour Cherry Baked Brie is wrapped in a plastic shrink wrap and has a white adhesive store label. UPC 0 217241 414996. The label is read in parts: "***SOUR CHERRY BAKED BRIE*** Puff Pastry (wheat flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid), malted barley flour, ascorbic acid, Shortening, Brie, Sour Cherries, Sugar, Water, Fruit Pectin, Citric, Lactic & Ascorbic Acid, Egg. CONTAINS: WHEAT, MILK, EGG***Remove from wrapping and bake at 400F until internal temperature reached 165F, about 25min***MARKETOFCHOICE.COM***".

FDA code information

Sell By dates up to and including 12/12/20.

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Full FDA record and distribution details

Original product description

Market of Choice brand Sour Cherry Baked Brie is wrapped in a plastic shrink wrap and has a white adhesive store label. UPC 0 217241 414996. The label is read in parts: "***SOUR CHERRY BAKED BRIE*** Puff Pastry (wheat flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid), malted barley flour, ascorbic acid, Shortening, Brie, Sour Cherries, Sugar, Water, Fruit Pectin, Citric, Lactic & Ascorbic Acid, Egg. CONTAINS: WHEAT, MILK, EGG***Remove from wrapping and bake at 400F until internal temperature reached 165F, about 25min***MARKETOFCHOICE.COM***".

Original FDA recall reason

Sour Cherry Baked Brie was recalled because the scale label, which was printed at retail stores, do not list almond.

Recall details

Recall number
F-0171-2021
Event ID
86928
FDA status
Terminated
Initiated
Dec 4, 2020
Reported
Dec 23, 2020
Classified
Dec 11, 2020
Terminated
Jan 6, 2021
Quantity
444 units
Location
Eugene, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed in Oregon

FDA source record · F-0171-2021

Data updated September 16, 2026. View official FDA data ↗

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