FDA Food recall ·
Frozen Raw Bulk 8 inch Blueberry Crumble Pie (4 pies/case) recall
- Recall number
- H-0550-2026
- Date
- (initiated February 19, 2026)
- Company / brand
- Willamette Valley Pie Company, LLC
1651 Eska Way, Silverton, OR, United States - Category
- Food › Class II
- Classification
- Class II
- Status
- Terminated
- Units affected
- 182 cases
- Hazard tags
- Listeria Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Frozen Raw Bulk 8 inch Blueberry Crumble Pie (4 pies/case). Net wt. 24.5oz. UPC 0002251881223. 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 pies were not sold to consumers at retail stores. Product is labeled with BAKING INSTRUCTIONS: Convection Oven: Preheat convection oven to 350 degrees F. Bake pies for 25 minutes. Reduce heat to 335 degrees. Bake for an additional 30-35 minutes. Ovens will vary. Adjust time and temperature accordingly. Conventional Oven: Preheat to 350 degrees F. Bake for 40-45 minutes. Suggestions: Brush a sugar wash, then sprinkle with turbinado sugar, or use egg wash before baking. For best results, allow to cool 3-4 hours.
Why was it recalled?
Potential contamination with listeria monocytogenes.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot 601926, Best By 1/19/2028.
Distribution
Distributed in IL and OR
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (food), recall H-0550-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.