Food Recall Check
Class II · Moderate risk Terminated Initiated May 28, 2025 (17 months ago)

Casa Mamita Churro Bites Filled with Chocolate Hazelnut Cream recall

Recalled by Camerican International Inc · Paramus, NJ, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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.

Undeclared allergen: Milk

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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

Quantity: 19,080 sell units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Alabama Florida Georgia Illinois Missouri Tennessee

FDA's distribution note: The recalled product was distributed to the following states: IL, TN, GA, FL,MO, AL

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Camerican International Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 28, 2025
In FDA report of
Aug 6, 2025
Terminated
Jan 9, 2026
FDA recall number
H-0349-2025 · event 96988
Official record
FDA enforcement report search

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