Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*1004497
Summary
The FDA issued a Class II for Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed by LAMB WESTON Inc. Reason: Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product..
Details
Source
Food Recall
External ID
F-0752-2025
Action Date
2025-05-14
Status
Terminated
Category
food
Product Description
Item M7204, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923813. Made in USA.
Lot/Code Info: USE THRU DATES: 2026.02.26 2026.02.27 2026.02.28 2026.03.01 2026.03.02 2026.04.15 2026.04.16 ***Codes*** 09502263 09502273 09502283 09503013 09503023 09504153 09504163
Quantity Affected: 7,929 cases
Reason for Recall
Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.
Distribution
Distributed in Arizona and Hawaii and including Japan, Kuwait, Taiwan, and UAE
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-19
Company
Richland, 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 22 food recalls issued in the same week, part of 204 food-related FDA actions this month.
LAMB WESTON Inc 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 Inc) 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 Inc have FDA actions?
LAMB WESTON Inc 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-0752-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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