Fresh Recalls

FDAClass II · Food · Recall H-0935-2026 · Recalled June 17, 2026

Cheesecake de Fresa [image] Strawberry Cheesecake The Original recall — Galaxy RG Corp

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Cheesecake de Fresa [image] Strawberry Cheesecake The Original
Company / brand
Galaxy RG
Lot / serial / date codes
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
Distribution
FL and TX.
Agency product description and boundaries

Cheesecake de Fresa [image] Strawberry Cheesecake The Original, Net Wt. 26 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852843

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Cheesecake de Fresa [image] Strawberry Cheesecake The Original

3. Open the official notice or contact

Official recall ID
H-0935-2026
Brand
Galaxy RG
Classification
Class II
Units affected
149 (26-oz) units
Recall status
Terminated
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Miami, FL, United States
Firm address
13815 Sw 139th Ct, N/A, 33186-5517

Identifying details (verbatim from the notice)

Product codes / lots
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
Distribution
FL and TX.
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
98732
Recall initiated
April 3, 2026
FDA classified
June 9, 2026
FDA report date
June 17, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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