Skip to main content
High RiskFDAfda-F-0093-2016UNDECLARED ALLERGEN

Traditional Round Yellow Tortillas. Sold under the brand names of: Better Made, Meijer, 7-Eleven Always Save & Wendy's. 3.75 oz, 12 oz, 1...

Category
Units Affected
5,954
Recall Date
September 30, 2015
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0093-2016.

Firm was notified by a customer that the product contained an undeclared milk allergen.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0093-2016.

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 Wyandot 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-0093-2016.

Wyandot 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

Wyandot Inc Recall FAQ

Wyandot Inc is the subject of a food safety report: Traditional Round Yellow Tortillas. Sold under the brand names of: Better Made, Meijer, 7-Eleven Always Save & Wendy's. 3.75 oz, 12 oz, 1.... The notice was published on September 30, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 5,954 units are potentially affected.