Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC 00022518893257. Handmade - Willamette
Summary
The FDA issued a Class II for Frozen Raw Bulk 9 inch Blueberry Crumble Pie ES (4 pies/case). Net wt. 38oz. UPC by Willamette Valley Pie Company, LLC. Reason: Potential contamination with listeria monocytogenes..
Details
Source
Food Recall
External ID
H-0551-2026
Action Date
2026-03-18
Status
Terminated
Category
food
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.
Lot/Code Info: Lot 601316, Best By 1/13/2028
Quantity Affected: 777 cases
Reason for Recall
Potential contamination with listeria monocytogenes.
Distribution
Distributed in IL and OR
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-19
Company
Silverton, OR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 35 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Willamette Valley Pie Company, LLC has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Willamette Valley Pie Company, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Willamette Valley Pie Company, LLC have FDA actions?
Willamette Valley Pie Company, LLC has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0551-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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