RecallHawk
Class II Recall

Casa Mamita, Churro Bites Filled with Chocolate Hazelnut Cream, 7.5 oz , Cardboard Box, 12 boxes per case, Keep Frozen U

Camerican International Inc

Summary

The FDA issued a Class II for Casa Mamita, Churro Bites Filled with Chocolate Hazelnut Cream, 7.5 oz , Cardboa by Camerican International Inc. Reason: Undeclared Allergen (Milk). Consumer found a breaded halloumi Cheese Stick in the bag of churro bites. The Halloumi Cheese contains milk which is not.

Details

Source

Food Recall

External ID

H-0349-2025

Action Date

2025-08-06

Status

Terminated

Category

food

Product Description

Casa Mamita, Churro Bites Filled with Chocolate Hazelnut Cream, 7.5 oz , Cardboard Box, 12 boxes per case, Keep Frozen Until Ready For Use

Lot/Code Info: Best By Date:7/14/2025 Lot Code 01425

Quantity Affected: 19,080 sell units

Reason for Recall

Undeclared Allergen (Milk). Consumer found a breaded halloumi Cheese Stick in the bag of churro bites. The Halloumi Cheese contains milk which is not an allergen in the churros.

Distribution

The recalled product was distributed to the following states: IL, TN, GA, FL,MO, AL

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-28

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

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 (Camerican International Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Camerican International Inc have FDA actions?

This is the only FDA action we have on record for Camerican International Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0349-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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