Domino Premium Pure Cane Golden Light Brown Sugar recall

Recalled by Domino Foods Inc · West Palm Beach, FL, United States

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

Why it was recalled

Possible foreign 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

Domino Premium Pure Cane Golden Light Brown Sugar, 50 LB bag, UPC 049200009727, Lots 50041 (Best By Jan 20, 2022), 50042 (Best By Jan 21, 2022), 50043 (Best By Jan 22, 2022)

Quantity: 3100 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.

Lots 50041 (Best By Jan 20, 2022), 50042 (Best By Jan 21, 2022), 50043 (Best By Jan 22, 2022)

Where it was sold

Alabama Arkansas Florida Georgia Iowa Illinois Kansas Kentucky Louisiana Michigan Minnesota Mississippi North Carolina North Dakota Nebraska New Mexico Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas Wisconsin

FDA's distribution note: Product was shipped to the following states: AL, AR, FL, GA, IA, IL, KS, KY, LA, MI, MN, MS, NE, NM, NC, ND, OH, OK, PA, SC, TN, TX, & WI. Product was also shipped to the following country: Saudi Arabia.

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: Domino Foods Inc
Initiated by: Voluntary: Firm initiated
Recall initiated: Feb 13, 2020
In FDA report of: Mar 4, 2020
Terminated: Nov 6, 2020
FDA recall number: F-0745-2020 · event 84988
Official record: FDA enforcement report search

Also recalled with it (7 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Foreign material Feb 13, 2020