RecallHawk
Class II Recall

PURE CANE GRANULATED SUGAR, NET WT 50 LB (22.67kg), Distributed by Domino Foods, Inc., Yonkers, NY 10705, STORE IN A COO

Domino Foods Inc

Summary

The FDA issued a Class II for PURE CANE GRANULATED SUGAR, NET WT 50 LB (22.67kg), Distributed by Domino Foods, by Domino Foods Inc. Reason: Potential contamination with foreign objects..

Details

Source

Food Recall

External ID

H-0637-2025

Action Date

2025-10-01

Status

Ongoing

Category

food

Product Description

PURE CANE GRANULATED SUGAR, NET WT 50 LB (22.67kg), Distributed by Domino Foods, Inc., Yonkers, NY 10705, STORE IN A COOL, DRY PLACE

Lot/Code Info: Lots: 75315A1, 75315B1, 75315C1, 75321A1, 75321B1, 75321C1; UPC: 015800030515; Item: 404736

Quantity Affected: 4,500 bags (50 lb/bag)

Reason for Recall

Potential contamination with foreign objects.

Distribution

CA, UT

Type: Voluntary: Firm initiated

Recall Initiated: 2025-08-12

Company

Domino Foods Inc

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 61 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 "H-0637-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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