Winco Foods Llc Recall: The product was found to be adulterated with Norovirus.

🇺🇸 United States

1. March 13, 2020 - Recall initiated
2. April 1, 2020 - Reported by source
3. May 20, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0857-2020

Event ID

85219

Status

Terminated

Classification

Class II

Company

Winco Foods Llc

Product description

WinCo Foods frozen Berry Medley (Strawberries, Blackberries, Raspberries and Blueberries), item# 107412, packaged in polyethylene bags. Product is distributed by WinCo Foods, LLC, Boise, ID 83704. Net weight 16 oz (1 lb or 454 g). UPC 70552 30522. Net weight 32 oz (2 lb or 907 g). UPC 70552 30512. The label is read in parts: "***WinCo FOODS*** Berry Medley***strawberries, blackberries, raspberries $ blueberries***KEEP FROZEN***".

Quantity

21,264 bags of Berry Medley.

Reason

The product was found to be adulterated with Norovirus.

Recall initiation date

March 13, 2020

Report date

April 1, 2020

Classification date

Not published in this source record

Termination date

May 20, 2020

Distribution pattern

Product was distributed in Arizona, California, Idaho, Montana, Nevada, Oklahoma, Oregon, Washington, Texas, and Utah.

UPC, lot, and code information

Best By Code DEC/9/21. Lot 4344905 Lot code breakdown as follows: 4 = IQF FACILITY 344 = JULIAN DATE (DECEMBER 10) 9 = YEAR 2019 05 = LINE # 5

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 85219 with 1 other product entry in Public Health Trace.

Responsible company: Winco Foods Llc

Other recalls from Winco Foods Llc

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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