FDA recall record

Willamette Valley Pie Company, LLC Frozen IQF Strawberries packed in a flexible polybag recall — FDA F-1229-2019

Frozen IQF strawberries are recalled due to potential contamination with Hepatitis A virus.

Class IIclassification
F-1229-2019official record ID
Apr 10, 2019report date

Recall record at a glance

Official recordF-1229-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmWillamette Valley Pie Company, LLC.
Report dateApr 10, 2019
Recall initiation dateFeb 7, 2019
Quantity1,448 cases (6/2 lb. bags per case)
LocationSilverton, OR, United States

Official product description

Frozen IQF Strawberries packed in a flexible polybag. Each bag is 2 lbs (906.5g), 6 bags per case. UPC is UPC: 0 22518 87710 3. The label of 2 lb. bag is read in parts: "***STRAWBERRIES***KEEP FROZEN***Net Weight 2 lbs. ***WILLAMETTE VALLEY FRUIT ***". The white adhesive label on the master case in read in parts: "***STRAWBERRIES ***QTY: 6/2 LB POLY-BAGS***ITEM CODE 0 22518 87710 3 *** KEEP FROZEN***LOT#: 255 811***BB: 09112020***Willamette Valley Fruit Co packed for Willamette Valley Pie Company 1651 Eska Way, Silverton OR 97381***ORIGIN: USA***".

Why the product was recalled

Frozen IQF strawberries are recalled due to potential contamination with Hepatitis A virus.

Distribution information

California, Oregon, Texas, and Washington.

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

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