Skip to main content
High RiskFDAfda-F-0568-2013UNDECLARED ALLERGEN

"***Productos El Gauchito Empanadillas Argentinas de Queso y Cebolla (Cheese and OnionTurnovers)***keep frozen or refrigerated***consumer...

Category
Units Affected
0
Recall Date
August 20, 2012
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0568-2013.

Undeclared soy, FD&C Yellow #6 and Red #40 contained in soft dough shells.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0568-2013.

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 Productos El Gauchito 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-0568-2013.

Productos El Gauchito

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

Productos El Gauchito Recall FAQ

Productos El Gauchito is the subject of a dairy safety report: "***Productos El Gauchito Empanadillas Argentinas de Queso y Cebolla (Cheese and OnionTurnovers)***keep frozen or refrigerated***consumer.... The notice was published on August 20, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 0 units are potentially affected.