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Class IITerminated in FDA datasetRecall initiated Nov 20, 2019

Lamb Weston Grown In Idaho Crispy Hash Brown Dices, packaged in 28 ounce poly retail bags, 6 or…

Recalling firm: Lamb Weston Inc

Why it was recalled

Crispy Hash Brown Dices product is recalled because it may contain pieces of hard rubber material.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 7, 2020.

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Compare the exact product and package details with the label you have.

ProductLamb Weston Grown In Idaho Crispy Hash Brown Dices, packaged in 28 ounce poly retail bags, 6 or 12 bags packaged in a master case. UPC: 0 43301 61170 4. The retail bag has the cooking instructions. Item #36003, Lamb Weston Grown in Idaho Crispy Hash Brown Dices, net wt. 21 lbs. master case. UPC 10043301611704. Item # 36603, Lamb Weston Grown in Idaho Crispy Hash Brown Dices, net wt. 10.5 lbs. master case. UPC 10043301611704.
Package size28 ounce
UPC043301611704

FDA code information

Lot 613008281HH, Best By: 022821.

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Full FDA record and distribution details

Original product description

Lamb Weston Grown In Idaho Crispy Hash Brown Dices, packaged in 28 ounce poly retail bags, 6 or 12 bags packaged in a master case. UPC: 0 43301 61170 4. The retail bag has the cooking instructions. Item #36003, Lamb Weston Grown in Idaho Crispy Hash Brown Dices, net wt. 21 lbs. master case. UPC 10043301611704. Item # 36603, Lamb Weston Grown in Idaho Crispy Hash Brown Dices, net wt. 10.5 lbs. master case. UPC 10043301611704.

Extracted codes and context

TypeCode / valueContext
UPC043301611704ged in 28 ounce poly retail bags, 6 or 12 bags packaged in a master case. UPC: 0 43301 61170 4. The retail bag has the cooking instructions. Item #36003, Lamb Weston Grown in Idaho Crispy Hash Brown Dices, net

Original FDA recall reason

Crispy Hash Brown Dices product is recalled because it may contain pieces of hard rubber material.

Recall details

Recall number
F-0344-2020
Event ID
84338
FDA status
Terminated
Initiated
Nov 20, 2019
Reported
Dec 11, 2019
Classified
Dec 18, 2019
Terminated
May 7, 2020
Quantity
total 6,062 cases (item #36003 = 1,700 cases and item #36603 = 4,362 cases)
Location
Twin Falls, ID, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

distributed in AZ, CA, CO, CT, GA, MA, MD, ME, NC, NY, OR, PA, TX, VA, and VT.

FDA source record · F-0344-2020

Data updated September 16, 2026. View official FDA data ↗

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