FDA recall record

Market of Choice Baked Brie Herb/Garlic recall — FDA F-0191-2016

Baked Brie Herb/Garlic was recalled due to undeclared pecans.

Class Iclassification
F-0191-2016official record ID
Nov 25, 2015report date

Recall record at a glance

Official recordF-0191-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMarket of Choice Inc.
Report dateNov 25, 2015
Recall initiation dateSep 30, 2015
Quantity24 units
LocationEugene, OR, United States

Official product description

Baked Brie Herb/Garlic. An 8 ounce portion of Baked Brie wrapped in Phyllo Dough with garlic and herbs. Product shipped frozen, but sold thawed in a cheese case. UPC 2 17563 01499 7

Why the product was recalled

Baked Brie Herb/Garlic was recalled due to undeclared pecans.

Distribution information

distributed in Oregon only

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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