Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 20, 2019 (7 years ago)

Lamb Weston Grown In Idaho Crispy Hash Brown Dices recall

Recalled by Lamb Weston Inc · Twin Falls, ID, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

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.

Quantity: total 6,062 cases (item #36003 = 1,700 cases and item #36603 = 4,362 cases)

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 613008281HH, Best By: 022821.

Where it was sold

Arizona California Colorado Connecticut Georgia Massachusetts Maryland Maine North Carolina New York Oregon Pennsylvania Texas Virginia Vermont

FDA's distribution note: distributed in AZ, CA, CO, CT, GA, MA, MD, ME, NC, NY, OR, PA, TX, VA, and VT.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Lamb Weston Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 20, 2019
In FDA report of
Dec 11, 2019
Terminated
May 7, 2020
FDA recall number
F-0344-2020 · event 84338
Official record
FDA enforcement report search

Other recalls by Lamb Weston Inc