Check the Batch
Class IITerminated in FDA datasetRecall initiated Oct 17, 2022

Domino and C&H Granulated Pure Cane Sugar Easy Baking Tub packaged in 3.5lb plastic tubs 6 tubs…

Recalling firm: Domino Foods Inc

Why it was recalled

Potential to contain metal wire from broken screen

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: Apr 14, 2023.

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

ProductDomino and C&H Granulated Pure Cane Sugar Easy Baking Tub packaged in 3.5lb plastic tubs 6 tubs per case
Package size3.5lb

FDA code information

Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25, 09/12/25 through 09/16/25, 10/10/25 through 10/14/25

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Domino and C&H Granulated Pure Cane Sugar Easy Baking Tub packaged in 3.5lb plastic tubs 6 tubs per case

Extracted codes and context

TypeCode / valueContext
lot52362Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 43
lot52363Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 B
lot52364Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By:
lot52365Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/
lot52371Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 thro
lot52372Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/
lot52373Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25,
lot52374Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25, 09/12/2
lot52375Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25, 09/12/25 throu
lot52411Lot Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25, 09/12/25 through 09/1
lot52412 Numbers: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25, 09/12/25 through 09/16/25, 1
lot52413s: 52362, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25, 09/12/25 through 09/16/25, 10/10/25
lot524142, 52363, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25, 09/12/25 through 09/16/25, 10/10/25 throug
lot524153, 52364, 52365, 52371, 52372, 52373, 52374, 52375, 52411, 52412, 52413, 52414, 52415 Product Numbers: 533031, 433478 Best By: 09/06/25 through 09/09/25, 09/12/25 through 09/16/25, 10/10/25 through 10/14

Original FDA recall reason

Potential to contain metal wire from broken screen

Recall details

Recall number
F-0082-2023
Event ID
91034
FDA status
Terminated
Initiated
Oct 17, 2022
Reported
Nov 9, 2022
Classified
Nov 1, 2022
Terminated
Apr 14, 2023
Quantity
6040 cases
Location
West Palm Beach, FL, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Product was distributed to distribution centers in the following states: Alabama, Arkansas, Connecticut, Georgia, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maine, Michigan, Missouri, Mississippi, North Carolina, Nebraska, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, Texas, Wisconsin

FDA source record · F-0082-2023

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

Follow official FDA and manufacturer guidance.