Class IITerminated in FDA datasetRecall initiated Feb 19, 2026

Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz.

Recalling firm: Willamette Valley Pie Company, LLC

Why it was recalled

Potential contamination with listeria monocytogenes.

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: Apr 3, 2026.

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ProductFrozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen raw pies were sold frozen in bulk packaging to grocery retailers' in-store bakeries. They are intended to be baked by the retailer before consumer sale. Frozen raw pies were not sold to consumers at retail stores. Product is labeled with BAKING INSTRUCTIONS: Preheat convection oven to 340 degrees Fahrenheit. Bake pies for 70-80 minutes. Ovens will vary. Adjust time and temperature accordingly to ensure center of pie reaches 210F.
Package size38oz

FDA code information

Lot 601316, Best By 1/13/2028

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Full FDA record and distribution details

Original product description

Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette Valley Pie Company LLC. 1651 Eska Way, Silverton, OR. Frozen raw pies were sold frozen in bulk packaging to grocery retailers' in-store bakeries. They are intended to be baked by the retailer before consumer sale. Frozen raw pies were not sold to consumers at retail stores. Product is labeled with BAKING INSTRUCTIONS: Preheat convection oven to 340 degrees Fahrenheit. Bake pies for 70-80 minutes. Ovens will vary. Adjust time and temperature accordingly to ensure center of pie reaches 210F.

Extracted codes and context

TypeCode / valueContext
best by1/13/2028Lot 601316, Best By 1/13/2028

Original FDA recall reason

Potential contamination with listeria monocytogenes.

Recall details

Recall number
H-0551-2026
Event ID
98466
FDA status
Terminated
Initiated
Feb 19, 2026
Reported
Mar 18, 2026
Classified
Mar 10, 2026
Terminated
Apr 3, 2026
Quantity
777 cases
Location
Silverton, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Distributed in IL and OR

FDA source record · H-0551-2026

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

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