Food Recall Check
Class I · High risk Terminated Initiated Oct 10, 2025 (12 months ago)

Casa Mamita Soft Taco Dinner Kit recall

Recalled by Teasdale Foods, Inc. · Louisville, KY, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared allergen - milk

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 Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g), UPC: 4099100318715, DIST. & SOLD EXCLUSIVELY BY: ALDI BATAVIA, IL 60510 Product consists of 10 flour tortillas, 1 sauce packet, and 1 seasoning packet within a carton; 6 cartons are packed into a mixed case with 6 additional hard taco dinner kits

Quantity: 3,654 cases (21,924 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.

Lot 25259, BEST IF USED BY MAR 15 26

Where it was sold

Alabama Connecticut Florida Indiana Maryland Michigan North Carolina New York Ohio Pennsylvania Wisconsin

FDA's distribution note: AL, CT, FL, IN, MD, MI, NC, NY, OH, PA, WI

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Teasdale Foods, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 10, 2025
In FDA report of
Nov 12, 2025
Terminated
Apr 29, 2026
FDA recall number
H-0156-2026 · event 97813
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.