Bulk Mexican sweet bread varieties including conchas, fino ellotes, fino curenos, danes ellotes, danes cuernos, bolillos
Summary
The FDA issued a Class II for Bulk Mexican sweet bread varieties including conchas, fino ellotes, fino curenos by EM Tortillas, LLC. Reason: Undeclared allergens; wheat, soy, and eggs..
Details
Source
Food Recall
External ID
F-0097-2025
Action Date
2024-11-13
Status
Terminated
Category
food
Product Description
Bulk Mexican sweet bread varieties including conchas, fino ellotes, fino curenos, danes ellotes, danes cuernos, bolillos, and teleras. Bakery products are packaged in unlabeled poly bags.
Lot/Code Info: 403-REG for conchas, finos, and Danes; 423-REG for teleras; 426-REG for bolillo
Quantity Affected: Collectively, 1,578 pieces
Reason for Recall
Undeclared allergens; wheat, soy, and eggs.
Distribution
CA
Type: Voluntary: Firm initiated
Recall Initiated: 2024-10-03
Company
Santa Ana, CA
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 55 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 (EM Tortillas, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does EM Tortillas, LLC have FDA actions?
This is the only FDA action we have on record for EM Tortillas, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0097-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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