Domino and C&H Granulated Pure Cane Sugar Easy Baking Tub packaged in 3.5lb plastic tubs 6 tubs per case
Summary
The FDA issued a Class II for Domino and C&H Granulated Pure Cane Sugar Easy Baking Tub packaged in 3.5lb plas by Domino Foods Inc. Reason: Potential to contain metal wire from broken screen.
Details
Source
Food Recall
External ID
F-0082-2023
Action Date
2022-11-09
Status
Terminated
Category
food
Product Description
Domino and C&H Granulated Pure Cane Sugar Easy Baking Tub packaged in 3.5lb plastic tubs 6 tubs per case
Lot/Code Info: 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
Quantity Affected: 6040 cases
Reason for Recall
Potential to contain metal wire from broken screen
Distribution
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
Type: Voluntary: Firm initiated
Recall Initiated: 2022-10-17
Company
West Palm Beach, FL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 58 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Domino Foods Inc has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Domino Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Domino Foods Inc have FDA actions?
Domino Foods Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0082-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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