Lamb Weston Sales Recall: Potential to be contaminated with Listeria monocytogenes.

🇺🇸 United States

1. August 19, 2022 - Recall initiated
2. October 5, 2022 - Reported by source
3. September 29, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1806-2022

Event ID

90746

Status

Terminated

Classification

Class II

Company

Lamb Weston Sales

Product description

Item GV020, Great Value Shredded Hash Browns, 4 lbs. bag, 6/4 lbs. bags per case. Product is frozen and it's not ready to eat. Distributed By: Walmart Inc. Bentonville, AR 72716. UPC 0 78742 15557 9. Product contains Potatoes, Disodium Dihydrogen Pyrophosphate, Dextrose.

Quantity

7,377 cases

Reason

Potential to be contaminated with Listeria monocytogenes.

Recall initiation date

August 19, 2022

Report date

October 5, 2022

Classification date

Not published in this source record

Termination date

September 29, 2023

Distribution pattern

Firm distributed products nationwide including Guam and foreign consignees are in Aruba, Bahrain, Bermuda, Canada, China, Costa Rica, Japan, Korea, Mexico, Panama, Singapore, and Taiwan.

UPC, lot, and code information

Lot Codes: 6180012524 6180012624 6180012724 6180031424

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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 90746 with 2 other product entries in Public Health Trace.

Responsible company: Lamb Weston Sales

Other recalls from Lamb Weston Sales

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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