Teasdale Foods, Inc. Recall: Undeclared allergen - milk

🇺🇸 United States

1. October 10, 2025 - Recall initiated
2. November 12, 2025 - Reported by source
3. April 29, 2026 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

H-0156-2026

Event ID

97813

Status

Terminated

Classification

Class I

Company

Teasdale Foods, Inc.

Product description

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)

Reason

Undeclared allergen - milk

Recall initiation date

October 10, 2025

Report date

November 12, 2025

Classification date

Not published in this source record

Termination date

April 29, 2026

Distribution pattern

AL, CT, FL, IN, MD, MI, NC, NY, OH, PA, WI

UPC, lot, and code information

UPC 4099100318715; Lot 25259, BEST IF USED BY MAR 15 26

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 97813 with 1 other product entry in Public Health Trace.

Responsible company: Teasdale Foods, Inc.

Other recalls from Teasdale Foods, Inc.

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Alabama	1
Connecticut	1
Florida	1
Indiana	1
Maryland	1
Michigan	1
North Carolina	1
New York	1
Ohio	1
Pennsylvania	1
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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