RecallHawk
Class II Recall

Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 24 oz (680g)) packaged in wax paper placed in clear bag and packed i

CATAO MARKET LLC

Summary

The FDA issued a Class II for Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 24 oz (680g)) packaged in wa by CATAO MARKET LLC. Reason: Undeclared colors FD&C Yellow #5.

Details

Source

Food Recall

External ID

H-0413-2026

Action Date

2026-01-28

Status

Terminated

Category

food

Product Description

Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 24 oz (680g)) packaged in wax paper placed in clear bag and packed in cardboard carton. 12/ 24 oz per master case.

Lot/Code Info: Product identified by Best By dates (12/18/2025 through 03/18/2026)

Quantity Affected: 520 master cases

Reason for Recall

Undeclared colors FD&C Yellow #5

Distribution

Product distributed only in FL.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-12-18

Company

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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.

CATAO MARKET LLC 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 (CATAO MARKET LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does CATAO MARKET LLC have FDA actions?

CATAO MARKET LLC 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-0413-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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