Skip to main content
High RiskFDAfda-F-1619-2013UNDECLARED ALLERGEN

Milagros Green Corn Tamales, packaged in plastic in quantities of one dozen

Category
Units Affected
95
Recall Date
June 28, 2013
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1619-2013.

Los Milagros Tortilleria is recalling Milagros Tortillas Green Corn Tamales because they did not list the sub-ingredient for Monterey Jack Cheese which contains the milk allergen.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1619-2013.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Los Milagros Tortilleria, Llc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1619-2013.

Los Milagros Tortilleria, LLC

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Los Milagros Tortilleria, Llc Recall FAQ

Los Milagros Tortilleria, Llc is the subject of a food safety report: Milagros Green Corn Tamales, packaged in plastic in quantities of one dozen. The notice was published on June 28, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 95 units are potentially affected.