50# (pound) Domino Light Brown Sugar. This is packaged in bags made of multiple ply kraft paper, and a poly liner. pro
Summary
The FDA issued a Class II for 50# (pound) Domino Light Brown Sugar. This is packaged in bags made of multiple by Domino Foods Inc. Reason: Syrup used to manufacture Light Brown Sugar may have been exposed to extraneous material, specifically a bird..
Details
Source
Food Recall
External ID
F-1404-2022
Action Date
2022-07-13
Status
Terminated
Category
food
Product Description
50# (pound) Domino Light Brown Sugar. This is packaged in bags made of multiple ply kraft paper, and a poly liner. product number is 403350
Lot/Code Info: Lots: 12241, 12242, 12243, 12244 UPC number: 049200009703
Quantity Affected: 3,150 bags
Reason for Recall
Syrup used to manufacture Light Brown Sugar may have been exposed to extraneous material, specifically a bird.
Distribution
NY, NJ, PA, RI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-18
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 53 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-1404-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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