Lamb Weston Inc Recall: Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.

🇺🇸 United States

1. April 19, 2025 - Recall initiated
2. May 14, 2025 - Reported by source
3. November 24, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0754-2025

Event ID

96738

Status

Terminated

Classification

Class II

Company

Lamb Weston Inc

Product description

Item M7414, frozen foodservice Lamb Weston Hashbrown Patties, frozen, LW Formed Oval 6/3.5LB bags per case. GTIN*10044979923820. Made in USA.

Quantity

2,079 cases

Reason

Approximately 1mm to 8 mm sized pieces of foreign material (plastic) found in product.

Recall initiation date

April 19, 2025

Report date

May 14, 2025

Classification date

Not published in this source record

Termination date

November 24, 2025

Distribution pattern

Distributed in Arizona and Hawaii and including Japan, Kuwait, Taiwan, and UAE

UPC, lot, and code information

USE THRU 16 MAR 2026 17 MAR 2026 18 MAR 2026 19 MAR 2026 20 MAR 2026 21 MAR 20262 25 MAR 20262 26 MAR 20262 29 MAR 20262 30 MAR 20262 31 MAR 20262 01 APR 20262 01 APR 20262 02 APR 20262 03 APR 20262 04 APR 20262 05 APR 20262 14 APR 20262 15 APR 20262 ***Codes*** 09503163, 09503173, 09503183, 09503193, 09503203, 09503213, 09503253, 09503263, 09503293, 09503303, 09503313, 09504013, 09504012, 09504022, 09504023, 09504033, 09504032, 09504042, 09504043, 09504053, 09504142, 09504153, 09504152

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 96738 with 3 other product entries in Public Health Trace.

Responsible company: Lamb Weston Inc

Other recalls from Lamb Weston Inc

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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