Skip to main content
RecallFDAfda-F-0817-2019CONTAMINATION

My Nanas Best Tasting Home Style-Estilo Casero Flour Tortillas Bakery Fresh. 24 oz (680g). Plastic bag

Category
Units Affected
894
Recall Date
January 22, 2019
Issuing Agency
Hazard
Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0817-2019.

Homestyle Estilo Casero tortillas are being recalled because the packaging ink is contaminating product.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0817-2019.

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 La Canasta Mexican Food Products, 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-0817-2019.

La Canasta Mexican Food Products, 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

La Canasta Mexican Food Products, Inc. Recall FAQ

La Canasta Mexican Food Products, Inc. is the subject of a food safety report: My Nanas Best Tasting Home Style-Estilo Casero Flour Tortillas Bakery Fresh. 24 oz (680g). Plastic bag. The notice was published on January 22, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 894 units are potentially affected.