Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g)
Recalled by Teasdale Foods, Inc.
Food recall
Teasdale Foods, Inc.
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
Teasdale Foods, Inc. has recalled Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g), according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on November 12, 2025 and was initiated on October 10, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g), with approximately 3,654 cases (21,924 units) affected. The company behind the recall is Teasdale Foods, Inc., based in Louisville, KY. The FDA describes the product as: “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…”
Why was Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g) recalled?
According to the FDA, the stated reason for the recall is: “Undeclared allergen - milk.” In plain terms, this recall relates to an undeclared ingredient or allergen.
An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.
What should you do?
If you think you may have bought Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g), compare it against the product description and identifying codes (Lot 25259, BEST IF USED BY MAR 15 26) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Teasdale Foods, Inc. or your local health authority.
About this recall
This recall was distributed in KY. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Terminated
- Date reported
- November 12, 2025
- Recall started
- October 10, 2025
- Distributed in
- KY
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g) recalled?+
According to the FDA: Undeclared allergen - milk
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have Casa Mamita Soft Taco Dinner Kit, Net Wt 13.4 OZ (379g)?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0156-2026. Information last synced from the FDA on July 5, 2026.