Market of Choice Inc Recall: Sour Cherry Baked Brie was recalled because the scale label, which was printed at retail stores, do not list almond.

🇺🇸 United States

1. December 4, 2020 - Recall initiated
2. December 23, 2020 - Reported by source
3. January 6, 2021 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0171-2021

Event ID

86928

Status

Terminated

Classification

Class I

Company

Market of Choice Inc

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***".

Quantity

444 units

Reason

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

Recall initiation date

December 4, 2020

Report date

December 23, 2020

Classification date

Not published in this source record

Termination date

January 6, 2021

Distribution pattern

distributed in Oregon

UPC, lot, and code information

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

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Market of Choice Inc

Other recalls from Market of Choice Inc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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