FDA recall record

Willamette Valley Pie Company, LLC packaged in clamshells container, six containers per case recall — FDA F-0970-2020

Cherry Pie packages were recalled due to being misbranded. The actual product inside clamshell package is Raspberry Rhubarb Pie, but it was mislabeled as…

Class IIclassification
F-0970-2020official record ID
May 27, 2020report date

Recall record at a glance

Official recordF-0970-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmWillamette Valley Pie Company, LLC.
Report dateMay 27, 2020
Recall initiation dateMay 13, 2020
Quantity48 units
LocationSilverton, OR, United States

Official product description

Willamette Valley Pie Company Cherry Pie, packaged in clamshells container, six containers per case. Each pie weighs 10 oz. and sold as individual pies to consumers. UPC: 0 22518 87916 9. The label on a clamshell container is read in parts: "***HANDMADE All-Natural Cherry Pie ***BAKED & READY TO EAT*** INGREDIENTS: Filling: Cherries, Organic Cane Sugar, Enriched Wheat Flour (wheat flour, malted barley flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid), Almond Extract (water, alcohol, oil of bitter almond), Cinnamon. Crust: Enriched Wheat Flour (wheat flour, niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid), Organic Palm Oil, Water, Organic Cane Sugar, Sea Salt. Contains: WHEAT, TREE NUTS (Almond)***". The label on a master CASE is read in parts: "***5" CHERRY PIE ***BAKED RETAIL***6 units/case***".

Why the product was recalled

Cherry Pie packages were recalled due to being misbranded. The actual product inside clamshell package is Raspberry Rhubarb Pie, but it was mislabeled as Cherry Pie. Raspberry Rhubarb Pie does NOT contain artificial almond extract.

Distribution information

distributed in Oregon only.

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: Telephone.

What to do next

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