FDA recall record

Willamette Valley Pie Company Bulk Frozen Cases: The 9" Vegan Pumpkin Pie bulk case has UPC recall — FDA F-0639-2024

Foreign object

Class IIclassification
F-0639-2024official record ID
Dec 27, 2023report date

Recall record at a glance

Official recordF-0639-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmWillamette Valley Pie Company, LLC
Report dateDec 27, 2023
Recall initiation dateNov 21, 2023
Quantity254 cases; 6 pies per case; 1,524 pies.
LocationSilverton, OR, United States

Official product description

Bulk Frozen Cases: The 9" Vegan Pumpkin Pie bulk case has UPC 22518 84081 and the label is read in parts: 9" Vegan Pumpkin Pie WFM, BAKED BULK, 6 units/case. KEEP FROZEN - TRANSPORT AND STORE AT LESS THAN ZERO DEGREES F. Just Thaw and serve. Remove from freezer, removed plastic wrap, and let thaw in REFRIGERATOR overnight. Please keep refrigerated. NOT SHELF STABLE. Willamette Valley Pie Company 1651 Eska Way, Silverton, OR 97381. Individual Retail Packages: Whole Foods Market - Vegan Pumpkin Pie, net Wt. 1lb 12oz (794g) packaged in window box or plastic clamshell. Whole Foods Market - Vegan Pumpkin Pie Half, net wt. 13 oz. (369g); packaged in plastic clamshell. Whole Foods Market - Vegan Pumpkin Pie Slice, net wt. 4 oz. (113g); packaged in plastic clamshell.

Why the product was recalled

Foreign object

Distribution information

Distributed in CA, IL, IN, KY, MI, MN, MO, NV, OH, OR, WA and WI.

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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