Cheesecake de Dulce de Leche [image] Caramel Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid
Summary
The FDA issued a Class II for Cheesecake de Dulce de Leche [image] Caramel Cheesecake The Original, Net Wt. 26 by Galaxy RG Corp. Reason: Undeclared colors (Yellow #5, Yellow #6, and/or Red #40)..
Details
Source
Food Recall
External ID
H-0933-2026
Action Date
2026-06-17
Status
Ongoing
Category
food
Product Description
Cheesecake de Dulce de Leche [image] Caramel Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852829
Lot/Code Info: Expiration Date: From 04/03/2026 to 05/03/2026 Lot#034320462, 034320562, 034320662, 034320962, 034321062, 034321162, 034321262, 034321362, 034321662, 034321762, 034321862, 034321962, 034322062, 034322362, 034322462, 034322562, 034322662, 034322762, 034323062, 034323162, 044320162, 044320262, 044320362
Quantity Affected: 498 (26-oz) units
Reason for Recall
Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).
Distribution
FL and TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-03
Company
Miami, 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 191 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Galaxy RG Corp has 23 FDA actions in our database, including 23 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 (Galaxy RG Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Galaxy RG Corp have FDA actions?
Galaxy RG Corp has 23 FDA actions in our database, including 23 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0933-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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