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