Item GV020, Great Value Shredded Hash Browns, 4 lbs. bag, 6/4 lbs. bags per case. Product is frozen and it's not ready
Summary
The FDA issued a Class II for Item GV020, Great Value Shredded Hash Browns, 4 lbs. bag, 6/4 lbs. bags per case by Lamb Weston Sales. Reason: Potential to be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1806-2022
Action Date
2022-10-05
Status
Terminated
Category
food
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.
Lot/Code Info: Lot Codes: 6180012524 6180012624 6180012724 6180031424
Quantity Affected: 7,377 cases
Reason for Recall
Potential to be contaminated with Listeria monocytogenes.
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-19
Company
Kennewick, WA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 76 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lamb Weston Sales has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lamb Weston Sales) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lamb Weston Sales have FDA actions?
Lamb Weston Sales has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1806-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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