Frozen Raw Bulk 8 inch Blueberry Crumble Pie recall
Recalled by Willamette Valley Pie Company, LLC
The product, as the FDA describes it: 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 it was recalled
Potential contamination with listeria monocytogenes.
The FDA has since closed this recall out, which means the company finished removing the product from sale. It is kept here because a closed recall still matters to anyone holding a package bought before it ended.
What to do if you have it
Nothing about frozen raw bulk 8 inch blueberry crumble pie will look or smell wrong, because the organisms behind this kind of recall leave no trace you can see or taste. Do not cook it to make it safe and do not sample it. Throw it out or return it, then wash anything it touched, including the shelf it sat on and the container beside it.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
Lot 601926, Best By 1/19/2028.
The details on record
| Recalling company | Willamette Valley Pie Company, LLC |
|---|---|
| Company location | Silverton, OR |
| Where it was distributed | Distributed in IL and OR |
| How much was recalled | 182 cases |
| Recall started | February 19, 2026 |
| Published by the FDA | March 18, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | |
| FDA recall number | H-0550-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
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