Class IITerminatedVoluntary: Firm initiated
EM Tortillas, LLC: food recall F-0097-2025
EM Tortillas, LLC of Santa Ana, CA recalled Bulk Mexican sweet bread varieties including conchas, fino ellotes, fino curenos, danes ellotes, danes cuernos,… Reason: Undeclared allergens; wheat, soy, and eggs. The FDA listed it as Class II in its Enforcement Report dated Nov 13, 2024; distribution: California.
Record status as published: Terminated (terminated Dec 17, 2024). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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.
- Product quantity
- Collectively, 1,578 pieces
- Reason for recall
- Undeclared allergens; wheat, soy, and eggs.
- Codes, lots and dates on the package
- 403-REG for conchas, finos, and Danes; 423-REG for teleras; 426-REG for bolillo
- Distribution pattern
- CA
- Recalling firm
- EM Tortillas, LLC, Santa Ana, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Oct 3, 2024 |
| Classified by the FDA | Nov 1, 2024 |
| Published in the Enforcement Report | Nov 13, 2024 |
| Terminated | Dec 17, 2024 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0097-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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