Skip to main content
RecallFDAfda-F-0828-2013OTHER

El Matador Mexican Style Salted Tortilla Chips 16oz (454 g) bags &32 oz (908 g) bags

Units Affected
16,956
Recall Date
November 1, 2012
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0828-2013.

Beginning 11/01/2012 Garden Fresh Gourmet recalled El Matador & Garden Fresh Gourmet Salted Tortilla Chips because quality standards of ingredients used in the products were not met.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0828-2013.

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 Garden Fresh Salsa, Inc. 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-0828-2013.

Garden Fresh Salsa, Inc.

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

Garden Fresh Salsa, Inc. Recall FAQ

Garden Fresh Salsa, Inc. is the subject of a snacks & candy safety report: El Matador Mexican Style Salted Tortilla Chips 16oz (454 g) bags &32 oz (908 g) bags. The notice was published on November 1, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 16,956 units are potentially affected.