RecallHawk
Class II Recall

Tortilla de mesa with 12 units per package, Tortilla Pirata with 10 units per package, Tortilla cruda especial with 20 u

Tortilleria Xpress Inc

Summary

The FDA issued a Class II for Tortilla de mesa with 12 units per package, Tortilla Pirata with 10 units per pa by Tortilleria Xpress Inc. Reason: Undeclared soy allergen.

Details

Source

Food Recall

External ID

H-0040-2025

Action Date

2025-06-18

Status

Completed

Category

food

Product Description

Tortilla de mesa with 12 units per package, Tortilla Pirata with 10 units per package, Tortilla cruda especial with 20 units per package, Tortilla Cruda Pirata with 20 units per package

Lot/Code Info: They are labeled with a date gun with the expiry.

Quantity Affected: 359 packages

Reason for Recall

Undeclared soy allergen

Distribution

Texas

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-06

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

How often does Tortilleria Xpress Inc have FDA actions?

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

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0040-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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