Recall record at a glance
| Official record | F-0842-2019 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Willamette Valley Pie Company, LLC. |
| Report date | Feb 13, 2019 |
| Recall initiation date | Dec 31, 2018 |
| Quantity | 850 cases (6/2 lb. bags per cases); 530 cases (2/5 lb. bags per case) |
| Location | Silverton, OR, United States |
Official product description
IQF Red Raspberries, packed in flexible poly bags, net wt. 2 lbs. per bag. There are six bags packed per case. UPC is 0 22518 87750 9. The label of 2 lb. bag is read in parts: "***Red Raspberries ***WILLAMETTE VALLEY FRUIT ***Ingredients: Red Raspberries*** 2994 82nd Avenue NE Salem, OR 97305***PRODUCT OF USA***". The white adhesive label on the master case in read in parts: "***IQF RED RASPBERRY***QTY: 6/2 LB POLY-BAGS***ITEM CODE 0 22518 87750 9 *** KEEP FROZEN***LOT#: 240 811***BB:08272020***Willamette Valley Fruit Co packed for Willamette Valley Pie Company 1651 Eska Way, Silverton OR 97381***ORIGIN: USA***". ***************** IQF Red Raspberries, packed in flexible poly bags, net wt. 5 lbs. per bag. There are two bags packed per case. UPC: 0 22518 87346 4. The label of 5 lb. bag is read in parts: "***WILLAMETTE VALLEY FRUIT *** 2994 82nd Avenue NE Salem, OR 97305******PRODUCT OF USA***". The white adhesive label on the master case in read in parts: "***IQF RED RASPBERRY***QTY: 5 / 2 LB POLY-BAGS***ITEM CODE 0 22518 87346 4 *** KEEP FROZEN***LOT#: 240 812***BB:08272020***Willamette Valley Fruit Co packed for Willamette Valley Pie Company 1651 Eska Way, Silverton OR 97381***ORIGIN: USA***".
Why the product was recalled
IQF Red Raspberries are recalled due to a potential contamination with Norovirus.
Distribution information
ID, CA, OR, TX, and WA.
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
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.